Antibody methods for selectively inhibiting VEGF

ABSTRACT

Disclosed are antibodies that specifically inhibit VEGF binding to only one (VEGFR2) of the two VEGF receptors. The antibodies effectively inhibit angiogenesis and induce tumor regression, and yet have improved safety due to their specificity. The present invention thus provides new antibody-based compositions, methods and combined protocols for treating cancer and other angiogenic diseases. Advantageous immunoconjugate and prodrug compositions and methods using the new VEGF-specific antibodies are also provided.

The present application claims priority to co-pending U.S. provisionalpatent application Serial No. 60/131,432, filed Apr. 28, 1999, theentire text and drawings of which application is specificallyincorporated by reference herein without disclaimer.

The U.S. Government owns rights in the present invention pursuant togrant numbers 1RO1 CA74951, 5RO CA54168 and T32 GM07062 from theNational Institutes of Health.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates generally to the fields of antibodies,angiogenesis and tumor treatment. More particularly, it providesanti-VEGF antibodies that specifically inhibit VEGF binding to only one(VEGFR2) of the two VEGF receptors. Such antibodies inhibit angiogenesisand induce tumor regression, and yet have improved safety due to theirspecific blocking properties. The antibody-based compositions andmethods of the invention also extend to the use of immunoconjugates andother therapeutic combinations, kits and methods, including those withprodrugs.

2. Description of the Related Art

Tumor cell resistance to chemotherapeutic agents represents asignificant problem in clinical oncology. In fact, this is one of themain reasons why many of the most prevalent forms of human cancer stillresist effective chemotherapeutic intervention, despite certain advancesin this field.

Another tumor treatment strategy is the use of an “immunotoxin”, inwhich an anti-tumor cell antibody is used to deliver a toxin to thetumor cells. However, in common with chemotherapeutic approaches,immunotoxin therapy also suffers from significant drawbacks when appliedto solid tumors. For example, antigen-negative or antigen-deficientcells can survive and repopulate the tumor or lead to furthermetastases.

A further reason for solid tumor resistance to antibody-based therapiesis that the tumor mass is generally impermeable to macromolecular agentssuch as antibodies and immunotoxins (Burrows et al., 1992; Dvorak etal., 1991a; Baxter and Jain, 1991). Both the physical diffusiondistances and the interstitial pressure within the tumor are significantlimitations to this type of therapy. Therefore, solid tumors, which makeup over 90% of all human cancers, have thus far proven resistant toantibody and immunotoxin treatment.

A more recent strategy has been to target the vasculature of solidtumors. Targeting the blood vessels of the tumors, rather than the tumorcells themselves, has certain advantages in that it is not likely tolead to the development of resistant tumor cells, and that the targetedcells are readily accessible. Moreover, destruction of the blood vesselsleads to an amplification of the anti-tumor effect, as many tumor cellsrely on a single vessel for their oxygen and nutrients (Burrows andThorpe, 1994a; 1994b). Exemplary vascular targeting strategies aredescribed in U.S. Pat. Nos. 5,855,866 and 5,965,132, which particularlydescribe the targeted delivery of anti-cellular agents and toxins tomarkers of tumor vasculature.

Another effective version of the vascular targeting approach is totarget a coagulation factor to a marker expressed or adsorbed within thetumor vasculature (Huang et al, 1997; U.S. Pat. Nos. 5,877,289,6,004,555, and 6,093,399. The delivery of coagulants, rather thantoxins, to tumor vasculature has the further advantages of reducedimmunogenicity and even lower risk of toxic side effects. As disclosedin U.S. Pat. No. 5,877,289, a preferred coagulation factor for use insuch tumor-specific “coaguligands” is a truncated version of the humancoagulation-inducing protein, Tissue Factor (TF), the major initiator ofblood coagulation.

Although the specific delivery of toxins and coagulation factors totumor blood vessels represents a significant advance in tumor treatment,certain peripheral tumor cells can survive the intratumoral destructioncaused by such therapies. Anti-angiogenic strategies would therefore beof use in combination with the tumor destruction methods of U.S. Pat.Nos. 5,855,866 and 5,877,289.

Anti-angiogenic tumor treatment strategies are based upon inhibiting theproliferation of budding vessels, generally at the periphery of a solidtumor. These therapies are mostly applied to reduce the risk ofmicrometastasis or to inhibit further growth of a solid tumor after moreconventional intervention (such as surgery or chemotherapy).

Angiogenesis is the development of new vasculature from preexistingblood vessels and/or circulating endothelial stem cells (Asahara et al.,1997; Springer et al., 1998; Folkman and Shing, 1992). Angiogenesisplays a vital role in many physiological processes, such asembryogenesis, wound healing and menstruation. Angiogenesis is alsoimportant in certain pathological events. In addition to a role in solidtumor growth and metastasis, other notable conditions with an angiogeniccomponent are arthritis, psoriasis and diabetic retinopathy (Hanahan andFolkman, 1996; Fidler and Ellis, 1994).

Angiogenesis is regulated in normal and malignant tissues by the balanceof angiogenic stimuli and angiogenic inhibitors that are produced in thetarget tissue and at distant sites (Fidler et al., 1998; McNamara etal., 1998). Vascular endothelial growth factor-A (VEGF, also known asvascular permeability factor, VPF) is a primary stimulant ofangiogenesis. VEGF is a multifunctional cytokine that is induced byhypoxia and oncogenic mutations and can be produced by a wide variety oftissues (Kerbel et al, 1998; Mazure et al., 1996).

The recognition of VEGF as a primary stimulus of angiogenesis inpathological conditions has led to various attempts to block VEGFactivity. Inhibitory anti-VEGF receptor antibodies, soluble receptorconstructs, antisense strategies, RNA aptamers against VEGF and lowmolecular weight VEGF receptor tyrosine kinase (RTK) inhibitors have allbeen proposed for use in interfering with VEGF signaling (Siemeister etal., 1998). In fact, monoclonal antibodies against VEGF have been shownto inhibit human tumor xenograft growth and ascites formation in mice(Kim et al., 1993; Asano et al., 1998; Mesiano et al., 1998; Luo et al.,1998a; 1998b; Borgstrom et al., 1996; 1998).

Although the foregoing studies underscore the importance of VEGF insolid tumor growth, and its potential as a target for tumor therapy, theidentification of additional agents that inhibit VEGF-inducedangiogenesis would be of benefit in expanding the number of therapeuticoptions. The development of therapeutic agents that more specificallyinhibit VEGF receptor binding would represent an important advance, solong as their anti-tumor effects w ere not substantially compromised bythe improved specificity.

SUMMARY OF THE INVENTION

The present invention overcomes certain drawbacks in the prior art byproviding new therapeutic compositions and methods for use inanti-angiogenic and anti-tumor treatment. The invention is based onantibodies that specifically inhibit VEGF binding to only one VEGFR2) ofthe two primary VEGF receptors. Such antibodies inhibit angiogenesis andinduce tumor regression as effectively as other anti-VEGF anti bodies,including those already in clinical trials, and yet have improved safetydue to their specific blocking properties. The compositions and methodsof the invention also extend to the use of immunoconjugates andcombinations, including prodrugs, using the specific category ofantibodies provided.

A particular advantage of the present invention is that the antibodiesprovided inhibit VEGF binding only to VEGFR, and not VEGFR1. Thiscontrasts with the leading antibodies in the prior art, includingA4.6.1, which inhibit VEGF binding to both VEGFR2 and VEGFR1. As VEGFR1has important biological roles unconnected to angiogenesis, particularlyin macrophage migration and chemotaxis, and osteoclast and chondroclastfunction, the present ability to inhibit only VEGFR2-mediatedangiogenesis is a distinct advantage. This translates into notableclinical benefits in that macrophages are still able to mediate hostanti-tumor responses and that bone metabolism, e.g., in the treatment ofpediatric cancers, is not adversely affected.

A further advantage is that, as binding of VEGF to VEGFR1 is maintainedin the presence of the antibodies of the invention, they can be used tospecifically deliver attached therapeutic agents to tumor vasculature byvirtue of binding to VEGF that is bound to VEGFR1, which is upregulatedon tumor endothelium. In the context of immunoconjugates, therefore, thepresent invention provides agents that have both anti-angiogenic andtumor destructive properties within the same molecule.

Yet a further advantage exists in the ability of the compositionsprovided to neutralize the survival signal of VEGF, which is mediatedthrough VEGFR2. The naked and conjugated antibodies of the inventionthus form synergistic combinations with other therapies and/or attachedagents, particularly those methods and agents that fail to achievemaximal effectiveness in vivo due to the ability of VEGF to counteracttheir destructive properties.

The present invention thus provides antibodies that specifically blockVEGF binding to the VEGFR2 receptor, or that block VEGF binding toessentially only the VEGFR2 receptor. Such antibodies significantlyinhibit VEGF binding to the VEGFR2 receptor (KDR/Flk-1) withoutsignificantly inhibiting VEGF binding to the VEGFR1 receptor (Flt-1).The antibodies thus inhibit VEGF binding to the VEGFR2 receptor(KDR/Flk-1), do not substantially inhibit VEGF binding to the VEGFR1receptor (Flt-1), exhibit anti-angiogenic and anti-tumor effects in vivoand do not significantly inhibit macrophage chemotaxis, osteoclast orchondroclast functions.

The antibodies of the invention are thus succinctly termed“VEGFR2-blocking, non-VEGFR1-blocking, anti-VEGF antibodies”. Even moresuccinctly, they are termed “VEGFR2-blocking, anti-VEGF antibodies”,which is used for simplicity in reference to all compositions, uses andmethods of the invention. A “VEGFR2-blocking, anti-VEGF antibody” is anantibody against VEGF that blocks VEGF binding to the VEGFR2 receptor.It will be clear that such antibodies are not antibodies against theVEGFR2 receptor itself.

Prior to the present invention, there was no motivation to generateanti-VEGF antibodies that specifically block VEGF binding to the VEGFR2receptor, but not the VEGFR1, neither were any advantages of suchantibodies envisioned. Importantly, as blocking antibodies need tophysically prevent the interaction of a growth factor and itsreceptor(s), and as receptor binding sites on growth factors are limitedin size, there was nothing to suggest that such specificVEGFR2-blocking, anti-VEGF antibodies could be developed.

However, in light of the inventors' surprising discoveries disclosedherein, the art is now provided with the knowledge that such specificinhibitory anti-VEGF antibodies can be prepared and have distinctadvantages. The present application further describes the methodologyfor generating candidate VEGFR2-blocking, anti-VEGF antibodies and theroutine technical aspects of the assays required to identify actualVEGFR2-blocking specific antibodies from the pool of candidates. Inlight of this invention, therefore, a range of VEGFR2-blocking,anti-VEGF antibodies can be made and used in a variety of embodiments,including in the inhibition of angiogenesis and the treatment ofangiogenic diseases and tumors without inhibiting VEGF signaling via theVEGFR1 receptor and without the notable drawbacks and side effectsassociated therewith.

As used throughout the entire application, the terms “a” and “an” areused in the sense that they mean “at least one”, “at least a first”,“one or more” or “a plurality” of the referenced components or steps,except in instances wherein an upper limit is thereafter specificallystated. Therefore, an“antibody”, as used herein, means “at least a firstantibody”. The operable limits and parameters of combinations, as withthe amounts of any single agent, will be known to those of ordinaryskill in the art in light of the present disclosure.

Antibodies that “specifically inhibit VEGF binding to the VEGF receptorVEGFR2 (KDR/Flk-1)” can now be identified by competition and/orfunctional assays. The preferred assays, for simplicity, are competitionassays based upon an ELISA. In competition assays, one pre-mixes oradmixes VEGF with varying amounts of the test antibodies (e.g., 100-foldto 1000-fold molar excess) and determines the ability of the testantibodies to reduce VEGF binding to VEGFR2. VEGF can be pre-labeled anddetected directly, or can be detected using a (secondary) anti-VEGFantibody or a secondary and tertiary antibody detection system. An ELISAformat of such a competition assay is a preferred format, but any typeof immunocompetition assay may be conducted.

VEGF binding to VEGFR2 in the presence of a completely irrelevantantibody (including non-blocking anti-VEGF monoclonal antibodies) is thecontrol high value (100%) in such a competition assay. In a test assay,a significant reduction in VEGF binding to VEGFR2 in the presence of atest antibody is indicative of a test antibody that significantlyinhibits VEGF binding to the VEGF receptor VEGFR2 (KDR/Flk-1).

A significant reduction is a “reproducible”, i.e., consistentlyobserved, reduction in binding. A “significant reduction” in terms ofthe present application is defined as a reproducible reduction (in VEGFbinding to VEGFR2) of at least about 45%, about 50%, about 55%, about60% or about 65% at any amount between about 100 fold and about 1000fold molar excess of antibody over VEGF.

As a preferred feature of the invention is that the antibodies provideddo not substantially inhibit VEGF binding to VEGFR1, antibodies thatexhibit a moderately significant reduction of VEGF binding to VEGFR2will still be useful, so long as they do not substantially inhibit VEGFbinding to VEGFR1. Nonetheless, more preferred antibodies will be thosethat have a more significant ability to inhibit VEGF binding to VEGFR2.These antibodies are those that exhibit a reproducible ability to reduceVEGF binding to VEGFR2 by at least about 70%, about 75% or about 80% atany amount between about 100 fold and about 1000 fold molar excess ofantibody over VEGF. Although not required to practice the invention,antibodies that reduce VEGF binding to VEGFR2 by at least about 85%,about 90%, about 95% or even higher are by no means excluded.

Anti-VEGF antibodies, or antigen-binding fragments thereof, that inhibitVEGF binding to the VEGF receptor VEGFR2 (KDR/Flk-1) withoutsignificantly inhibiting VEGF binding to the VEGF receptor VEGFR1(Flt-1) are readily confirmed by simple competition assays such as thosedescribed above, but using VEGFR1.

Absence of a significant reduction is a “reproducible”, i.e.,consistently observed, “substantial maintenance of binding”. A“substantial maintenance of binding” in terms of the present applicationis defined as a reproducible maintenance (in VEGF binding to VEGFR1) ofat least about 60%, about 75%, about 80% or about 85% at any amountbetween about 100 fold and about 1000 fold molar excess of antibody overVEGF.

The intention of using antibodies that do not substantially inhibit VEGFbinding to VEGFR1 is to maintain the biological functions mediated byVEGFR1. Therefore, an antibody need only maintain sufficient VEGFbinding to VEGFR1 so that a biological response is induced by VEGF.Nonetheless, more preferred antibodies will be those that have a moresignificant ability to maintain VEGF binding to VEGFR1. These antibodiesare those that exhibit a reproducible ability to maintain VEGF bindingto VEGFR1 at levels of at least about 88%, about 90%, about 92%, about95% or of about 98-99% at any amount between about 100 fold and about1000 fold molar excess of antibody over VEGF.

It will be understood that antibodies that more substantially inhibitVEGF binding to VEGFR2 can likely tolerate more reduction in bindingVEGFR1. Equally, where an antibody has a moderate reduction in VEGFbinding to VEGFR2, the maintenance of binding to VEGFR1 should be morestringently pursued.

Another preferred binding assay to identify and/or confirm that anantibody inhibits VEGF binding to the VEGF receptor VEGFR2 (KDR/Flk-1)is a co-precipitation assay. A co-precipitation assay tests the abilityof an antibody to block the binding of VEGF to one or more receptors insolution. In such an assay, VEGF or detectably-labeled VEGF is incubatedwith a suitable form of the receptor.

There are many formats for conducting immunoprecipitation orco-precipitation assays. In the present case, a “suitable form of thereceptor” may be the VEGFR2 receptor at issue or the extracellulardomain of the receptor. Immunoprecipitation with then require, as wellas the standard reagents, the presence of an antibody against the VEGFR2receptor or an epitope on the extracellular domain of the receptordistinct from the site to which VEGF binds. The present inventionprovides other “suitable” forms of the VEGF receptors, namely theextracellular domains of the receptors linked to an Fc antibody portion.Such receptor/Fc constructs can be precipitated by incubation with aneffective immunoprecipitating composition, such as a Protein A-basedcomposition.

Irrespective of the suitable receptor, the immunoprecipitation orco-precipitation assays are preferably conducted with controls. Theability of VEGF alone to bind to the chosen receptor should be confirmedby precipitation in the absence of an anti-VEGF antibody. Preferably,parallel incubations are conducted in the presence or absence of anantibody with known binding properties to act as a control. Mostpreferably, assays using both a blocking control and non-blockingcontrol antibody are run in parallel.

Any bound immunological species are then immunoprecipitated, e.g., byincubation with an effective immunoprecipitating composition, such as aProtein A composition or Protein A sepharose beads. The precipitate isthen tested for the presence of VEGF. Where the VEGF in the initialincubation was detectably-labeled VEGF, such as radio-labeled VEGF, anyVEGF in the immunoprecipitates can be detected directly. Any non-labeledVEGF in the immunoprecipitates may be detected by other suitable means,e.g., by gel separation and immunodetection with an anti-VEGF antibody.

The ability of an antibody to block VEGF binding to a VEGF receptor,such as VEGFR2, in such a co-precipitation assay can be readilyquantitated, although qualitative results are also valuable.Quantification can be achieved by direct measurement of labeled VEGF ore.g., by densitometric analyses of immunodetected VEGF. Antibodies thatexhibit a reproducible, i.e., consistently observed, ability to inhibitVEGF binding to VEGFR2 can thus be detected, and useful antibodies canbe chosen according to the quantitative criteria outlined above.

Anti-VEGF antibodies that do not significantly inhibit VEGF binding tothe VEGF receptor VEGFR1 (Flt-1) can also be readily identified byconducting co-precipitation assays as described above, but using VEGFR1rather than VEGFR. Therefore, anti-VEGF antibodies that inhibit VEGFbinding to the VEGF receptor VEGFR2 (KDR/Flk-1) without significantlyinhibiting VEGF binding to the VEGF receptor VEGFR1 (Flt-1) can also bereadily identified using such methods.

The present application also provides various functional assays toidentify and/or confirm that an antibody significantly inhibits VEGFbinding to the VEGF receptor VEGFR2 (KDR/Flk-1). These are generallyrelated to the identification of VEGFR2 as the receptor responsible forcertain defined biological responses. Although less preferred than theforegoing competition-type assays, which are conducted in cell-freesystems and are most reproducible, reliable, labor-saving andcost-effective, the following assays are nonetheless useful in thecontext of the present invention.

For example, a VEGFR2-blocking, anti-VEGF antibody may be identified bytesting for the ability to inhibit VEGF-mediated endothelial cell growth(inhibiting the mitogenic activity of VEGF). Any suitable assay may beemployed using any of a variety of endothelial cells in the presence ofVEGF with or without test antibodies. Preferably, duplicate assays arerun in parallel, such as those without VEGF and those with controlantibodies of defined properties (both blocking and non-blocking).Endothelial cell growth may be determined and preferably accuratelyquantified by any acceptable means of determining cell number, includingcolorimetric assays.

An antibody with an ability to inhibit VEGF-mediated endothelial cellgrowth will generally exhibit a consistently observed inhibition ofVEGF-mediated endothelial cell growth of about 25%, 30%, 35%, 40% 45% or50% or so. Inhibition in such ranges will indicate an antibody withproperties sufficient to inhibit angiogenesis in vivo. Antibodies withmore significant inhibitory activity are not excluded from theinvention.

Further functional assays to identify antibodies in accordance with thepresent invention are assays to test blocking of VEGF-inducedphosphorylation. Any suitable assay may be employed using any of avariety of endothelial cells that express any form of native orrecombinant phosphorylatable VEGFR2. Cells are incubated with VEGF inthe presence or absence of the antibody to be tested for a suitable timeperiod. Preferably, duplicate assays are run in parallel, such as thosewithout VEGF and those with control antibodies of defined properties(both blocking and non-blocking).

VEGF-induced phosphorylation of VEGFR2 may be determined and preferablyaccurately quantified by any acceptable means. Generally, VEGFR2 isimmunoprecipitated for further analyses. The degree of phosphorylationof VEGFR2 may be determined directly, for example, the cells may havebeen incubated with ³²P-labelled ATP, allowing direct quantification ofthe ³²P within the immunoprecipitated VEGFR2. Preferably, theimmunoprecipitated VEGFR2 are analyzed by other means, e.g., by gelseparation and immunodetection with an antibody that binds tophosphotyrosine residues. An antibody with an ability to inhibitVEGF-induced phosphorylation of VEGFR2 will generally exhibit aconsistently observed reduction in the levels of phosphorylated VEGFR2.

Yet further functional assays to identify VEGFR2-blocking, anti-VEGFantibodies in accordance with the present invention are assays to testinhibition of VEGF-induced vascular permeability. Although any suchassay may be used, a particularly suitable assay is the Milespermeability assay, wherein animals such as guinea pigs are injectedwith a dye, such as Evan's blue dye, and the appearance of the dye inthe animal skin is determined after the provision of VEGF in thepresence or absence of test antibodies. Preferably, duplicate studiesare conducted in parallel, such as those without VEGF and those withcontrol antibodies of defined properties (both blocking andnon-blocking). The appearance of dye in the animal skin is typically asspots, such as blue spots, in the back of the animal, which can bephotographed and measured.

VEGFR2-blocking, anti-VEGF antibodies will inhibit VEGF-induced-vascularpermeability as a consistently observed inhibition at lowconcentrations, such as when provided at a 100-fold, or 1000-fold molarexcess over VEGF. Antibodies that do not block VEGF binding to VEGFR2will not show any significant inhibition of VEGF induced-vascularpermeability. Generally, antibodies that block VEGF-induced permeabilityonly at high concentrations, such as at a 10-fold molar excess overVEGF, will not be antibodies with properties in accordance with thepresent invention.

Widely accepted functional assays of angiogenesis and, hence,anti-angiogenic agents are the corneal micropocket assay ofneovascularization and the chick chorio-allantoic membrane assay (CAM)assay. U.S. Pat. No. 5,712,291 is specifically incorporated herein byreference to show that the corneal micropocket and CAM assays aresufficiently predictive to identify agents for use in the treatment ofan extremely wide range of angiogenic diseases.

U.S. Pat. No. 5,001,116 is also specifically incorporated herein byreference for purposes of describing the CAM assay. Essentially,fertilized chick embryos are removed from their shell on day 3 or 4, anda methylcellulose disc containing the test compound is implanted on thechorioallantoic membrane. The embryos are examined approximately 48hours later and, if a clear avascular zone appears around themethylcellulose disc, the diameter of that zone is measured. Asdisclosed in U.S. Pat. No. 5,712,291, specifically incorporated hereinby reference for this purpose, in the context of the present invention,the appearance of any avascular zone is sufficient to evidence ananti-angiogenic antibody. The larger the zone, the more effective theantibody.

The corneal micropocket assay of neovascularization may be practicedusing rat or rabbit corneas. This in vivo model is widely accepted asbeing predictive of clinical usefulness, as evidenced by U.S. Pat. Nos.5,712,291 and 5,871,723, each specifically incorporated herein byreference for evidence purposes. Although not believed to beparticularly relevant the present invention, the corneal assays arepreferable over the CAM assay because they will generally recognizecompounds that are inactive per se but are metabolized to yield activecompounds.

In the present invention, the corneal micropocket assay is used toidentify an anti-angiogenic agent. This is evidenced by a significantreduction in angiogenesis, as represented by a consistently observed andpreferably marked reduction in the number of blood vessels within thecornea. Such responses are preferably defined as those corneas showingonly an occasional sprout and/or hairpin loop that displayed no evidenceof sustained growth when contacted with the test substance.

Exemplary VEGFR2-blocking, anti-VEGF antibodies (and antigen-bindingfragments) of the invention include those that:

(a) significantly inhibit VEGF binding to the VEGF receptor VEGFR2(KDR/Flk-1);

(b) do not significantly inhibit VEGF binding to the VEGF receptorVEGFR1 (Flt-1);

(c) inhibit, and preferably, significantly inhibit, VEGF-inducedphosphorylation of VEGFR2;

(d) inhibit, and preferably, significantly inhibit, VEGF-inducedvascular permeability;

(e) inhibit, and preferably, significantly inhibit, VEGF-mediatedendothelial cell proliferation;

(f) inhibit, and preferably, significantly inhibit, angiogenesis;

(g) do not significantly inhibit VEGFR1-mediated stimulation oractivation of macrophages, osteoclasts or chondroclasts; and

(h) localize to tumor vasculature and tumor stroma upon administrationto an animal with a vascularized tumor.

A particular aspect of the invention is based on the inventors'original, surprising discovery of antibodies that specifically inhibitedVEGF binding to the VEGFR2 receptor, that had significant anti-tumoreffects in vivo and that did not inhibit VEGF binding to the VEGFR1receptor. In certain embodiments, the present invention thus providesantibodies of defined epitope-specificity, wherein such antibodies, orantigen-binding fragments thereof, bind to essentially the same epitopeas the monoclonal antibody 2C3 (ATCC PTA 1595).

The invention as claimed is enabled in accordance with the presentspecification and readily available technological references, know-howand starting materials. Nonetheless, a sample of the hybridoma cell lineproducing the 2C3 monoclonal antibody was submitted Mar. 27, for receiptMar. 28, 2000, for deposit with the American Type Culture Collection(ATCC), 10801 University Blvd., Manassas, Va. 20110-2209, U.S.A. andgiven ATCC Accession number ATCC PTA 1595 on Apr. 11, 2000. This depositwas made under the provisions of the Budapest Treaty on theInternational Recognition of the Deposit of Microorganisms for thePurposes of Patent Procedure and the regulations thereof (BudapestTreaty). The hybridoma will be made available by the ATCC under theterms of the Budapest Treaty upon issue of a U.S. patent with pertinentclaims. Availability of the deposited hybridoma is not to be construedas a license to practice the invention in contravention of the rightsgranted under the authority of any government in accordance with itspatent laws.

Certain preferred compositions are therefore compositions comprising atleast a first anti-VEGF antibody, or antigen-binding fragment thereof,or at least a first purified anti-VEGF antibody, or antigen-bindingfragment thereof, that binds to substantially the same epitope as themonoclonal antibody 2C3 (ATCC PTA 1595); compositions comprising atleast a first monoclonal antibody, or antigen-binding fragment thereof,that binds to VEGF at essentially the same epitope as the monoclonalantibody 2C3 (ATCC PTA 1595); and compositions comprising at least afirst anti-VEGF monoclonal antibody, or antigen-binding fragmentthereof, that binds to the same epitope as the monoclonal antibody 2C3(ATCC PTA 1595).

Notwithstanding, certain other compositions, antibodies, methods, andparticularly first and second medical uses of the invention, concernanti-VEGF antibodies, or antigen-binding fragments thereof, that bind tothe same, or substantially the same, epitope as the monoclonal antibody2C3 (ATCC PTA 1595) other than the monoclonal antibody 2C3 (ATCC PTA1595) itself.

The terms “that bind to about, substantially or essentially the same, orthe same, epitope as” the monoclonal antibody 2C3 (ATCC PTA 1595) meanthat an antibody “cross-reacts” with the monoclonal antibody 2C3 (ATCCPTA 1595). “Cross-reactive antibodies” are those that recognize, bind toor have immunospecificity for substantially or essentially the same, orthe same, epitope or “epitopic site” as the monoclonal antibody 2C3(ATCC PTA 1595) such that are able to effectively compete with themonoclonal antibody 2C3 (ATCC PTA 1595) for binding to VEGF.“2C3-cross-reactive antibodies” are succinctly termed “2C3-likeantibodies” and “2C3-based antibodies”, and such terms are usedinterchangeably herein and apply to compositions, uses and methods.

The identification of one or more antibodies that bind(s) to about,substantially, essentially or at the same epitope as the monoclonalantibody 2C3 (ATCC PTA 1595) is a straightforward technical matter nowthat 2C3, with its advantageous properties, has been provided. As theidentification of cross-reactive antibodies is determined in comparisonto a reference antibody, it will be understood that actually determiningthe epitope to which the reference antibody (2C3) and the test antibodybind is not in any way required in order to identify an antibody thatbinds to the same or substantially the same epitope as the monoclonalantibody 2C3. However, considerable information on the epitope bound by2C3 is included herein and epitope mapping can be further performed, asdescribed by Champe et al. (1995, specifically incorporated herein byreference).

The identification of cross-reactive antibodies can be readilydetermined using any one of variety of immunological screening assays inwhich antibody competition can be assessed. All such assays are routinein the art and are further described herein in detail. U.S. Pat. No.5,660,827, issued Aug. 26, 1997, is specifically incorporated herein byreference for purposes including even further supplementing the presentteaching concerning how to make antibodies that bind to the same orsubstantially the same epitope as a given antibody, such as 2C3.

For example, where the test antibodies to be examined are obtained fromdifferent source animals, or are even of a different isotype, a simplecompetition assay may be employed in which the control (2C3) and testantibodies are admixed (or pre-adsorbed) and applied to a VEGF antigencomposition. By “VEGF antigen composition” is meant any composition thatcontains a 2C3-binding VEGF antigen as described herein, such as freeVEGF. Thus, protocols based upon ELISAs and Western blotting aresuitable for use in such simple competition studies.

In certain embodiments, one would or pre-mix the control antibodies(2C3) with varying amounts of the test antibodies (e.g., 1:10 or 1:100)for a period of time prior to applying to an antigen composition. Inother embodiments, the control and varying amounts of test antibodiescan simply be admixed during exposure to the antigen composition In anyevent, by using species or isotype secondary antibodies one will be ableto detect only the bound control antibodies, the binding of which willbe reduced by the presence of a test antibody that recognizessubstantially the same epitope.

In conducting an antibody competition study between a control antibodyand any test antibody (irrespective of species or isotype), one mayfirst label the control (2C3) with a detectable label, such as, e.g.,biotin or an enzymatic (or even radioactive) label to enable subsequentidentification. In these cases, one would pre-mix or incubate thelabeled control antibodies with the test antibodies to be examined atvarious ratios (e.g., 1:10 or 1:100) and (optionally after a suitableperiod of time) then assay the reactivity of the labeled controlantibodies and compare this with a control value in which no potentiallycompeting test antibody was included in the incubation.

The assay may again be any one of a range of immunological assays basedupon antibody hybridization, and the control antibodies would bedetected by means of detecting their label, e.g., using streptavidin inthe case of biotinylated antibodies or by using a chromogenic substratein connection with an enzymatic label (such as3,3′5,5′-tetramethylbenzidine (TMB) substrate with peroxidase enzyme) orby simply detecting a radioactive label. An antibody that binds to thesame epitope as the control antibodies will be able to effectivelycompete for binding and thus will significantly reduce control antibodybinding, as evidenced by a reduction in bound label.

The reactivity of the (labeled) control antibodies in the absence of acompletely irrelevant antibody would be the control high value. Thecontrol low value would be obtained by incubating the labeled (2C3)antibodies with unlabelled antibodies of exactly the same type (2C3),when competition would occur and reduce binding of the labeledantibodies. In a test assay, a significant reduction in labeled antibodyreactivity in the presence of a test antibody is indicative of a testantibody that recognizes the same epitope, i.e., one that “cross-reacts”with the labeled (2C3) antibody.

A significant reduction is a “reproducible”, i.e., consistentlyobserved, reduction in binding. A “significant reduction” in terms ofthe present application is defined as a reproducible reduction (in 2C3binding to VEGF in an ELISA) of at least about 70%, about 75% or about80% at any ratio between about 1:10 and about 1:100. Antibodies witheven more stringent cross-blocking activities will exhibit areproducible reduction (in 2C3 binding to VEGF in an ELISA or othersuitable assay) of at least about 82%, about 85%, about 88%, about 90%,about 92% or about 95% or so at any ratio between about 1:10 and about1:100. Complete or near-complete cross-blocking, such as exhibiting areproducible reduction in 2C3 binding to VEGF of about 99%, about 98%,about 97% or about 96% or so, although by no means required to practicethe invention, is certainly not excluded.

The invention is exemplified by monoclonal antibody 2C3, produced byhybridoma ATCC PTA 1595, or an antigen-binding fragment of such amonoclonal antibody. A hybridoma that produces a monoclonal anti-VEGFantibody that binds to substantially the same epitope as the monoclonalantibody 2C3 (ATCC PTA 1595) is another aspect of the invention.

The invention further provides anti-VEGF antibodies that bind tosubstantially the same epitope as the monoclonal antibody 2C3 (ATCC PTA1595), prepared by a process comprising immunizing an animal with atleast a first immunogenic VEGF component and selecting from theimmunized animal an antibody that substantially cross-reacts with themonoclonal antibody 2C3 (ATCC PTA 1595); and anti-VEGF antibodies thatbind to substantially the same epitope as the monoclonal antibody 2C3(ATCC PTA 1595), prepared by a process comprising immunizing an animalwith at least a first immunogenic VEGF component and selecting across-reactive anti-VEGF antibody from the immunized animal byidentifying an antibody that substantially reduces the binding of the2C3 antibody to VEGF.

Anti-VEGF antibodies, or antigen-binding fragments thereof, that bind tosubstantially the same epitope as the monoclonal antibody 2C3 (ATCC PTA1595) and that specifically inhibits VEGF binding to the VEGF receptorVEGFR2 (KDR/Flk-1); and anti-VEGF antibodies, or antigen-bindingfragments thereof, that bind to substantially the same epitope as themonoclonal antibody 2C3 (ATCC PTA 1595) and that inhibits VEGF bindingto the VEGF receptor VEGFR2 (KDR/Flk-1) without significantly inhibitingVEGF binding to the VEGF receptor VEGFR1 (Flt-1) form other aspects ofthe invention.

Antibodies with such combinations of properties can be readilyidentified by one or more or a combination of the receptor competition,ELISA, co-precipitation, and/or functional assays and the2C3-crossreactivity assays described above. The guidance concerning thequantitative assessment of 2C3-like antibodies that consistentlysignificantly reduce VEGF binding to VEGFR2 and that consistently do notsignificantly inhibit VEGF binding to VEGFR1 is as described above.

2C3 is herein shown reduce the amount VEGF that bound to VEGFR2-coatedELISA wells to about 26% and 19%, respectively, at 100 fold and 1000fold molar excesses over VEGF. These figures equate to reductions inVEGF binding to VEGFR2 of about 74% and about 81%, respectively. 2C3 isherein shown maintain the amount VEGF that bound to VEGFR2-coated ELISAwells at about 92% and 105%, respectively, at 100 fold and 1000 foldmolar excesses over VEGF.

It will again be understood that 2C3-like or crossreactive antibodiesthat more substantially inhibit VEGF binding to VEGFR2 can likelytolerate more reduction in binding VEGFR1. Equally, where an antibodyhas a moderate reduction in VEGF binding to VEGFR2, the maintenance ofbinding to VEGFR1 should be more stringently pursued.

Additional exemplary anti-VEGF antibodies (and antigen-bindingfragments) of the invention are therefore those that:

(a) bind to a non-conformationally dependent VEGF epitope, as assessedby binding to VEGF in a Western blot;

(b) bind to free VEGF;

(c) significantly inhibit VEGF binding to the VEGF receptor VEGFR2(KDR/Flk-1);

(d) do not significantly inhibit VEGF binding to the VEGF receptorVEGFR1 (Flt-1);

(e) inhibit, and preferably, significantly inhibit, VEGF-inducedphosphorylation of VEGFR2;

(f) inhibit, and preferably, significantly inhibit, VEGF-inducedvascular permeability;

(g) inhibit, and preferably, significantly inhibit, VEGF-mediatedendothelial cell proliferation;

(h) inhibit, and preferably, significantly inhibit, angiogenesis;

(i) do not significantly inhibit VEGFR1-mediated stimulation oractivation of macrophages, osteoclasts or chondroclasts;

(j) localize to tumor vasculature and tumor stroma upon administrationto an animal with a vascularized tumor; and

(k) bind to the same or substantially the same epitope as the monoclonalantibody 2C3 (ATCC PTA 1595).

In the following descriptions of the compositions, immunoconjugates,pharmaceuticals, combinations, cocktails, kits, first and second medicaluses and all methods in accordance with this invention, the terms“antibody” and “immunoconjugate”, or an antigen-binding region thereof,unless otherwise specifically stated or made clear from the scientificterminology, refer to a range of VEGFR2-blocking, anti-VEGF antibodiesas well as to specific 2C3-cross-reactive antibodies.

The terms “antibody” and “immunoglobulin”, as used herein, refer broadlyto any immunological binding agent, including polyclonal and monoclonalantibodies. Depending on the type of constant domain in the heavychains, antibodies are assigned to one of five major classes: IgA, IgD,IgE, IgG, and IgM. Several of these are further divided into subclassesor isotypes, such as IgG1, IgG2, IgG3, IgG4, and the like. Theheavy-chain constant domains that correspond to the difference classesof immunoglobulins are termed α, δ, ε, γ and μ, respectively. Thesubunit structures and three-dimensional configurations of differentclasses of immunoglobulins are well known.

Generally, where antibodies rather than antigen binding regions are usedin the invention, IgG and/or IgM are preferred because they are the mostcommon antibodies in the physiological situation and because they aremost easily made in a laboratory setting.

The “light chains” of mammalian antibodies are assigned to one of twoclearly distinct types: kappa (κ) and lambda (λ), based on the aminoacid sequences of their constant domains. There is essentially nopreference to the use of κ0 or λ light chains in the antibodies of thepresent invention.

The use of monoclonal antibodies (MAbs) or derivatives thereof is muchpreferred. MAbs are recognized to have certain advantages, e.g.,reproducibility and large-scale production, that makes them suitable forclinical treatment. The invention thus provides monoclonal antibodies ofthe murine, human, monkey, rat, hamster, rabbit and even frog or chickenorigin. Murine, human or humanized monoclonal antibodies will generallybe preferred.

As will be understood by those in the art, the immunological bindingreagents encompassed by the term “antibody” extend to all antibodiesfrom all species, and antigen binding fragments thereof, includingdimeric, trimeric and multimeric antibodies; bispecific antibodies;chimeric antibodies; human and humanized antibodies; recombinant andengineered antibodies, and fragments thereof.

The term “antibody” is thus used to refer to any antibody-like moleculethat has an antigen binding region, and this term includes antibodyfragments such as Fab′, Fab. F(ab′)₂, single domain antibodies (DABs),Fv, scFv (single chain Fv), linear antibodies, diabodies, and the like.The techniques for preparing and using various antibody-based constructsand fragments are well known in the art (see Kabat et al., 1991,specifically incorporated herein by reference). Diabodies, inparticular, are further described in EP 404, 097 and WO 93/11161, eachspecifically incorporated herein by reference; whereas linear antibodiesare farther described in Zapata et al. (1995), specifically incorporatedherein by reference.

In certain embodiments, the compositions of the invention comprise atleast a first anti-VEGF antibody that comprises at least a firstvariable region that includes an amino acid sequence region of at leastabout 75%, more preferably, at least about 80%, more preferably, atleast about 85%, more preferably, at least about 90% and mostpreferably, at least about 95% or so amino acid sequence identity to theamino acid sequence of SEQ ID NO:7 or SEQ ID NO:9; wherein saidanti-VEGF antibody at least substantially maintains the biologicalproperties of the VEGFR2-blocking, anti-VEGF antibodies of the presentinvention, as exemplified by the 2C3 antibody.

Identity or homology with respect to these and other anti-VEGF antibodysequences of the present invention is defined herein as the percentageof amino acid residues in a candidate sequence that are identical to thesequences of SEQ ID NO:7 or SEQ ID NO:9, or to the sequence of anotheranti-VEGF antibody of the invention, after aligning the sequences andintroducing gaps, if necessary, to achieve the maximum percent sequenceidentity. The maintenance of substantially the same, or even moreeffective biological properties of the VEGFR2-blocking, anti-VEGFantibody used for the sequence comparison is particularly important.Such comparisons are easily conducted, e.g., using one or more of thevarious assays described in detail herein.

In certain preferred embodiments, anti-VEGF antibodies of the inventioncomprise at least a first variable region that includes an amino acidsequence region having the amino acid sequence of SEQ ID NO:7 or SEQ IDNO:9, as exemplified by variable regions that include an amino acidsequence region encoded by the nucleic acid sequences of SEQ ID NO:6 orSEQ ID NO:8. Such sequences are the sequences of Vh and Vκ of the 2C3ScFv encompassing CDR1-3 (complementarity determining regions) of thevariable regions of the heavy and light chains.

In other preferred embodiments, second generation antibodies areprovided that have enhanced or superior properties in comparison to anoriginal VEGFR2-blocking, anti-VEGF antibody, such as 2C3. For example,the second generation antibodies may have a stronger binding affinity,more effective blocking of VEGF binding to VEGFR2, more specificblocking of VEGF binding to VEGFR2, even less blocking of VEGF bindingto VEGFR1, enhanced ability to inhibit VEGF-induced proliferation and/ormigration of endothelial cells, superior ability to inhibit,VEGF-induced vascular permeability, and preferably, an increased abilityto inhibit VEGF-induced angiogenesis in vivo, and to treat angiogenicdiseases, including vascularized tumors.

Comparisons to identify effective second generation antibodies arereadily conducted and quantified, e.g., using one or more of the variousassays described in detail herein. Second generation antibodies thathave an enhanced biological property or activity of at least about10-fold, preferably, at least about 20-fold, and more preferably, atleast about 50-fold, in comparison to the VEGF2-blocking, anti-VEGFantibodies of the present invention, as exemplified by the 2C3 antibody,are encompassed by the present invention. 1 5

In certain embodiments, the antibodies employed will be “humanized”,part-human or human antibodies. “Humanized” antibodies are generallychimeric monoclonal antibodies from mouse, rat, or other non-humanspecies, bearing human constant and/or variable region domains(“part-human chimeric antibodies”). Various humanized monoclonalantibodies for use in the present invention will be chimeric antibodieswherein at least a first antigen binding region, or complementaritydetermining region (CDR), of a mouse, rat or other non-human monoclonalantibody is operatively attached to, or “grafted” onto, a human antibodyconstant region or “framework”.

“Humanized” monoclonal antibodies for use herein may also be monoclonalantibodies from non-human species wherein one or more selected aminoacids have been exchanged for amino acids more commonly observed inhuman antibodies. This can be readily achieved through the use ofroutine recombinant technology, particularly site-specific mutagenesis.

Entirely human, rather than “humanized” ⁹, antibodies may also beprepared and used in the present invention. Such human antibodies may beobtained from healthy subjects by simply obtaining a population of mixedperipheral blood lymphocytes from a human subject, includingantigen-presenting and antibody-producing cells, and stimulating thecell population in vitro by admixing with an immunogenically effectiveamount of a VEGF sample. The human anti-VEGF antibody-producing cells,once obtained, are used in hybridoma and/or recombinant antibodyproduction.

Further techniques for human monoclonal antibody production includeimmunizing a transgenic animal, preferably a transgenic mouse, whichcomprises a human antibody library with an immunogenically effectiveamount of a VEGF sample. This also generates human anti-VEGFantibody-producing cells for further manipulation in hybridoma and/orrecombinant antibody production, with the advantage that spleen cells,rather than peripheral blood cells, can be readily obtained from thetransgenic animal or mouse.

VEGFR2-blocking, anti-VEGF antibodies in accordance with the inventionmay be readily prepared by processes and methods that comprise:

(a) preparing candidate antibody-producing cells; and

(b) selecting from the candidate antibody-producing cells an antibodythat significantly inhibits VEGF binding to VEGFR2 (KDR/Flk-1) and doesnot significantly inhibit VEGF binding to the VEGF receptor VEGFR1(Flt-1l).

Other antibodies in accordance with the invention may be readilyprepared by selecting an antibody that substantially cross-reacts withthe monoclonal antibody 2C3 (ATCC PTA 1595). Suitable preparativeprocesses and methods comprise:

(a) preparing candidate antibody-producing cells; and

(b) selecting from the candidate antibody-producing cells an antibodythat substantially cross-reacts with the monoclonal antibody 2C3 (ATCCPTA 1595).

One processes of preparing suitable antibody-producing cells andobtaining antibodies therefrom may be conduced in situ in a givenpatient. That is, simply providing an immunogenically effective amountof an immunogenic VEGF sample to a patient will result in appropriateantibody generation. Thus, the antibody is still “obtained” from theantibody-producing cell, but it does not have to be isolated away from ahost and subsequently provided to a patient, being able to spontaneouslylocalize to the tumor vasculature and exert its biological anti-tumoreffects. However, such embodiments are not preferred due to the markedlack of specificity.

Suitable antibody-producing cells may also be obtained, and antibodiessubsequently isolated and/or purified, by stimulating peripheral bloodlymphocytes with VEGF in vitro.

Other methods comprise administering to an animal an immunizingcomposition comprising at least a first immunogenic VEGF component andselecting from the immunized animal an antibody that significantlyinhibits VEGF binding to VEGFR2 (KDR/Flk-1) and does not significantlyinhibit VEGF binding to the VEGF receptor VEGFR1 (Flt-1), and optionallythat substantially cross-reacts with the monoclonal antibody 2C3 (ATCCPTA 1595). These methods generally comprise:

(a) immunizing an animal by administering to the animal at least onedose, and optionally more than one dose, of an immunogenically effectiveamount of an immunogenic VEGF sample (such as a first human VEGFcomponent, a substantially full length VEGF component, or recombinanthuman VEGF); and

(b) obtaining a suitable antibody-producing cell from the immunizedanimal, such as an antibody-producing cell that produces an antibodythat significantly inhibits VEGF binding to VEGFR2 (KDR/Flk-1) and doesnot significantly inhibit VEGF binding to the VEGF receptor VEGFR1(Flt-1), and optionally that substantially cross-reacts with themonoclonal antibody 2C3 (ATCC PTA 1595).

The immunogenically effective amount of the VEGF sample or samples maybe administered as VEGF conjugates, or in combination with any suitableadjuvant, such as Freund's complete adjuvant. Any empirical technique orvariation may be employed to increase immunogenicity. Intact,substantially full length human VEGF is generally preferred as animmunogen.

Irrespective of the nature of the immunization process, or the type ofimmunized animal, suitable antibody-producing cells are obtained fromthe immunized animal and, preferably, further manipulated by the hand ofman. “An immunized animal”, as used herein, is a non-human animal,unless otherwise expressly stated. Although any antibody-producing cellmay be used, most preferably, spleen cells are obtained as the source ofthe antibody-producing cells. The antibody-producing cells may be usedin a preparative process that comprises:

(a) fusing a suitable anti-VEGF antibody-producing cell with an immortalcell to prepare a hybridoma that produces a monoclonal antibody inaccordance with the present invention; and

(b) obtaining a suitable anti-VEGF antibody in accordance with theinvention from the hybridoma. “Suitable” anti-VEGF antibody-producingcells, hybridomas and antibodies are those that produce, or exist as,VEGFR2-blocking, anti-VEGF antibodies, i.e., antibodies thatsignificantly inhibit VEGF binding to VEGFR2 (KDR/Flk-1) and do notsignificantly inhibit VEGF binding to the VEGF receptor VEGFR1 (Flt-1),and optionally, that substantially cross-react with the monoclonalantibody 2C3 (ATCC PTA 1595).

Hybridoma-based monoclonal antibody preparative methods thus includethose that comprise:

(a) immunizing an animal by administering to the animal at least onedose, and optionally more than one dose, of an immunogenically effectiveamount of an immunogenic VEGF sample, preferably an intact human VEGFsample;

(b) preparing a collection of monoclonal antibody-producing hybridomasfrom the immunized animal;

(c) selecting from the collection at least a first hybridoma thatproduces at least a first VEGFR2-blocking, anti-VEGF monoclonal antibodyin accordance with the invention, optionally an anti-VEGF antibody thatsubstantially cross-reacts with the monoclonal antibody 2C3 (ATCC PTA1595); and

(d) culturing the at least a first antibody-producing hybridoma toprovide the at least a first VEGFR2-blocking, anti-VEGF monoclonalantibody; and preferably

(e) obtaining the at least a first VEGFR2-blocking, anti-VEGF monoclonalantibody from the cultured at least a first hybridoma.

In identifying an anti-VEGF antibody that substantially cross-reactswith the monoclonal antibody 2C3 (ATCC PTA 1595), the selecting step maycomprise:

(a) contacting a VEGF sample with effective amounts of the monoclonalantibody 2C3 (ATCC PTA 1595) and a candidate antibody; and

(b) determining the ability of the candidate antibody to substantiallyreduce the binding of the 2C3 antibody to the VEGF sample; wherein theability of a candidate antibody to substantially reduce the binding ofthe 2C3 antibody to the VEGF sample is indicative of an anti-VEGFantibody that binds to substantially the same epitope as the monoclonalantibody 2C3 (ATCC PTA 1595).

The selecting step may further comprise:

(a) contacting a first VEGF sample with an effective binding amount ofthe monoclonal antibody 2C3 (ATCC PTA 1595) and determining the amountof 2C3 that binds to VEGF;

(b) contacting a second VEGF sample with an effective binding amount ofthe monoclonal antibody 2C3 (ATCC PTA 1595) in combination with aneffective competing amount of a candidate antibody and determining theamount of 2C3 that binds to VEGF in the presence of the candidateantibody; and

(c) identifying an anti-VEGF antibody that binds to substantially thesame epitope as the monoclonal antibody 2C3 (ATCC PTA 1595) by selectinga candidate antibody that reduces the amount of 2C3 that binds to VEGFby, preferably, at least about 80%.

As non-human animals are used for immunization, the monoclonalantibodies obtained from such a hybridoma will often have a non-humanmake up. Such antibodies may be optionally subjected to a humanizationprocess, grafting or mutation, as known to those of skill in the art andfurther disclosed herein. Alternatively, transgenic animals, such asmice, may be used that comprise a human antibody gene library.Immunization of such animals will therefore directly result in thegeneration of suitable human antibodies.

After the production of a suitable antibody-producing cell, mostpreferably a hybridoma, whether producing human or non-human antibodies,the monoclonal antibody-encoding nucleic acids may be cloned to preparea “recombinant” monoclonal antibody. Any recombinant cloning techniquemay be utilized, including the use of PCR™ to prime the synthesis of theantibody-encoding nucleic acid sequences. Therefore, yet furtherappropriate monoclonal antibody preparative methods include those thatcomprise using the antibody-producing cells as follows:

(a) obtaining at least a first suitable anti-VEGF antibody-encodingnucleic acid molecule or segment from a suitable anti-VEGFantibody-producing cell, preferably a hybridoma; and

(b) expressing the nucleic acid molecule or segment in a recombinanthost cell to obtain a recombinant VEGFR2-blocking, anti-VEGF monoclonalantibody in accordance with the present invention.

However, other powerful recombinant techniques are available that areideally suited to the preparation of recombinant monoclonal antibodies.Such recombinant techniques include the phagemid library-basedmonoclonal antibody preparative methods comprising:

(a) immunizing an animal by administering to the animal at least onedose, and optionally more than one dose, of an immunogenically effectiveamount of an immunogenic VEGF sample (such as an intact human VEGFsample);

(b) preparing a combinatorial immunoglobulin phagemid library expressingRNA isolated from the antibody-producing cells, preferably from thespleen. of the immunized animal;

(c) selecting from the phagemid library at least a first clone thatexpresses at least a first VEGFR2-blocking, anti-VEGF antibody,optionally one that substantially cross-reacts with the monoclonalantibody 2C3 (ATCC PTA 1595);

(d) obtaining VEGFR2-blocking, anti-VEGF antibody-encoding nucleic acidsfrom the at least a first selected clone and expressing the nucleicacids in a recombinant host cell to provide the at least a firstVEGFR2-blocking, anti-VEGF antibody; and preferably

(e) obtaining the at least a first VEGFR2-blocking, anti-VEGF antibodyexpressed by the nucleic acids obtained from the at least a firstselected clone.

Again, in such phagemid library-based techniques, transgenic animalsbearing human antibody gene libraries may be employed, thus yieldingrecombinant human monoclonal antibodies.

Irrespective of the manner of preparation of a first VEGFR2-blocking,anti-VEGF antibody nucleic acid segment, further suitable antibodynucleic acid segments may be readily prepared by standard molecularbiological techniques. In order to confirm that any variant, mutant orsecond generation VEGFR2-blocking, anti-VEGF antibody nucleic acidsegment is suitable for use in the present invention, the nucleic acidsegment will be tested to confirm expression of a VEGFR2-blocking,anti-VEGF antibody in accordance with the present invention. Preferably,the variant, mutant or second generation nucleic acid segment will alsobe tested to confirm hybridization under standard, more preferably,standard stringent hybridization conditions. Exemplary suitablehybridization conditions include hybridization in about 7% sodiumdodecyl sulfate (SDS), about 0.5 M NaPO₄, about 1 mM EDTA at about 50°C.; and washing with about 1% SDS at about 42° C.

As a variety of recombinant monoclonal antibodies, whether human ornon-human in origin, may be readily prepared, the treatment methods ofthe invention may be executed by providing to the animal or patient atleast a first nucleic acid segment that expresses a biologicallyeffective amount of at least a first VEGFR2-blocking, anti-VEGF antibodyin the patient. The “nucleic acid segment that expresses aVEGFR2-blocking, anti-VEGF, 2C3-like or 2C3-based antibody” willgenerally be in the form of at least an expression construct, and may bein the form of an expression construct comprised within a virus orwithin a recombinant host cell. Preferred gene therapy vectors of thepresent invention will generally be viral vectors, such as comprisedwithin a recombinant retrovirus, herpes simplex virus (HSV), adenovirus,adeno-associated virus (AAV), cytomegalovirus (CMV), and the like.

This invention further provides compositions comprising at least a firstpurified VEGFR2-blocking, anti-VEGF antibody, or antigen-bindingfragment thereof, optionally one that binds to essentially the sameepitope as the monoclonal antibody 2C3 (ATCC PTA 1595). Suchcompositions may be pharmaceutically acceptable compositions orcompositions for use in laboratory studies. In terms of thepharmaceutical compositions, they may preferably be formulated forparenteral administration, such as for intravenous administration.

The present invention provides a number of methods and uses of theVEGFR2-blocking, anti-VEGF antibodies, including the 2C3-cross-reactive,2C3-like or 2C3-based antibodies. Concerning all methods, the terms “a”and “an” are used to mean “at least one”, “at least a first”, “one ormore” or “a plurality” of steps in the recited methods, except wherespecifically stated. This is particularly relevant to the administrationsteps in the treatment methods. Thus, not only may different doses beemployed with the present invention, but different numbers of doses,e.g., injections, may be used, up to and including multiple injections.Combined therapeutics may be used, administered before, after or duringadministration of the anti-VEGF therapeutic antibody.

Various useful in vitro methods and uses are provided that haveimportant biological implications. First provided are methods of, anduses in, binding VEGF, which generally comprise effectively contacting acomposition comprising VEGF, preferably free (non-receptor bound) VEGFwith at least a first VEGFR2-blocking, anti-VEGF antibody, orantigen-binding fragment thereof, optionally an antibody that binds tosubstantially the same epitope as the monoclonal antibody 2C3 (ATCC PTA1595).

Methods of, and uses in, detecting VEGF are provided, which generallycomprise contacting a composition suspected of containing VEGF with atleast a first VEGFR2-blocking, anti-VEGF antibody, or antigen-bindingfragment thereof, optionally one that binds to substantially the sameepitope as the monoclonal antibody 2C3 (ATCC PTA 1595), under conditionseffective to allow the formation of VEGF/antibody complexes anddetecting the complexes so formed. The detection methods and uses may beused in connection with biological samples, e.g., in diagnostics forangiogenesis and tumors, and diagnostic kits based thereon are alsoprovided.

The present invention provides methods of, and uses in, preferentiallyor specifically inhibiting VEGF binding to the VEGF receptor VEGFR2,which generally comprise contacting, in the presence of VEGF, apopulation of cells or tissues that includes endothelial cells thatexpress VEGFR2 (KDR/Flk-1) with a composition comprising a biologicallyeffective amount of at least a first VEGFR2-blocking, anti-VEGFantibody, optionally one that binds to substantially the same epitope asthe monoclonal antibody 2C3 (ATCC PTA 1595), or an antigen-bindingfragment thereof, under conditions effective to inhibit VEGF binding tothe VEGF receptor VEGFR2.

Methods of, and uses in, significantly inhibiting VEGF binding to theVEGF receptor VEGFR2, without significantly inhibiting VEGF binding tothe VEGF receptor VEGFR1 are provided. These methods comprisecontacting, in the presence of VEGF, a population of cells or tissuesthat includes a population of endothelial cells that express VEGFR2(KDR/Flk-1) and VEGFR1 (Flt-1) with a composition comprising abiologically effective amount of at least a first VEGFR2-blocking,anti-VEGF antibody, optionally an anti-VEGF antibody that binds tosubstantially the same epitope as the monoclonal antibody 2C3 (ATCC PTA1595), or an antigen-binding fragment thereof, under conditionseffective to inhibit VEGF binding to the VEGF receptor VEGFR2, withoutsignificantly inhibiting VEGF binding to the VEGF receptor VEGFR1.

Further methods and uses of the invention are in analyzing thebiological roles of the VEGF receptors termed VEGFR2 and VEGFR1,comprising the steps of:

(a) contacting a biological composition or tissue that comprises VEGFand a population of cells that express VEGFR2 (KDR/Flk-1) and VEGFR1(Flt-1) receptors with a composition comprising a biologically effectiveamount of at least a first VEGFR2-blocking, anti-VEGF antibody,optionally an anti-VEGF antibody that binds to substantially the sameepitope as the monoclonal antibody 2C3 (ATCC PTA 1595), or anantigen-binding fragment thereof; and

(b) determining the effect of the VEGFR2-blocking, anti-VEGF antibody onat least a first biological response to VEGF; wherein:

(i) an alteration in a biological response in the presence of theVEGFR2-blocking, anti-VEGF antibody is indicative of a response mediatedby the VEGFR2 receptor; and

(ii) the maintenance of a biological response in the presence of theVEGFR2-blocking, anti-VEGF antibody is indicative of a response mediatedby the VEGFR1 receptor.

Proliferation inhibition methods and uses are provided, including thoseto specifically inhibit VEGF-induced endothelial cell proliferationand/or migration, which generally comprise contacting a population ofcells or tissues that includes a population of endothelial cells andVEGF with a composition comprising a biologically effective amount of atleast a first VEGFR2-blocking, anti-VEGF antibody, optionally one thatbinds to substantially the same epitope as the monoclonal antibody2C3(ATCC PTA 1595), or an antigen-binding fragment of the VEGFR2-blocking,anti-VEGF antibody, under conditions effective to inhibit VEGF-inducedendothelial cell proliferation and/or migration.

Methods of, and uses in, inhibiting VEGF-induced endothelial cellproliferation and/or migration, without significantly inhibitingVEGF-induced macrophage chemotaxis are provided, which generallycomprise contacting a population of cells or tissues that containsendothelial cells, macrophages and VEGF with a composition comprising abiologically effective amount of at least a first VEGFR2-blocking,anti-VEGF antibody, optionally one that binds to substantially the sameepitope as the monoclonal antibody 2C3 (ATCC PTA 1595), or anantigen-binding fragment of the anti-VEGF antibody, under conditionseffective to inhibit VEGF-induced endothelial cell proliferation and/ormigration, without significantly inhibiting VEGF-induced macrophagechemotaxis.

Methods of, and uses in, inhibiting VEGF-induced endothelial cellproliferation and/or migration and, optionally, angiogenesis, withoutsignificantly inhibiting VEGF stimulation of macrophages, osteoclasts orchondroclasts are further provided. The methods generally comprisecontacting a population of cells or tissues that contain endothelialcells and at least one of macrophages, osteoclasts or chondroclasts,with a composition comprising a biologically effective amount of atleast a first VEGFR2-blocking, anti-VEGF antibody, optionally one thatbinds to substantially the same epitope as the monoclonal antibody 2C3(ATCC PTA 1595), or an antigen-binding fragment of the antibody, underconditions effective to inhibit VEGF-induced endothelial cellproliferation and/or migration or angiogenesis, without significantlyinhibiting VEGF stimulation of macrophages, osteoclasts orchondroclasts.

The foregoing methods and uses can be performed in vitro and in vivo, inthe latter case, wherein the tissues or cells are located within ananimal and the anti-VEGF antibody is administered to the animal. In bothcases, the methods and uses become methods and uses for inhibitingangiogenesis, comprising contacting a tissue comprising, or a populationof, potentially angiogenic blood vessels, i.e., those potentiallyexposed to VEGF, with an anti-angiogenic composition comprising abiologically effective amount of at least a first VEGFR-blocking,anti-VEGF antibody, optionally one that binds to substantially the sameepitope as the monoclonal antibody 2C3 (ATCC PTA 1595), or anantigen-binding fragment thereof, under conditions effective to inhibitangiogenesis.

Where populations of potentially angiogenic blood vessels are maintainedex vivo, the present invention has utility in drug discovery programs.In vitro screening assays, with reliable positive and negative controls,are useful as a first step in the development of drugs to inhibit orpromoter angiogenesis, as well as in the delineation of furtherinformation on the angiogenic process. Where the population ofpotentially angiogenic blood vessels is located within an animal orpatient, the anti-angiogenic composition is administered to the animalas a form of therapy.

“Biologically effective amounts”, in terms of each of the foregoinginhibitory methods are therefore amounts of VEGFR2-blocking, anti-VEGFantibodies, optionally 2C3-based antibodies, effective to inhibitVEGF-induced endothelial cell proliferation and/or migration; to inhibitVEGF-induced endothelial cell proliferation and/or migration, withoutsignificantly inhibiting VEGF-induced macrophage chemotaxis; to inhibitVEGF-induced endothelial cell proliferation and/or migration orangiogenesis, without significantly inhibiting VEGF stimulation ofmacrophages, osteoclasts or chondroclasts; and, overall, to reducevascular endothelial cell proliferation and/or migration in a mannereffective to inhibit blood vessels growth or angiogenesis.

The invention thus provides methods of, and uses in, inhibitingVEGF-induced angiogenesis and, preferably, treating an angiogenicdisease, without significantly inhibiting VEGF stimulation ofmacrophages, osteoclasts or chondroclasts. The methods generallycomprise contacting a population of cells or tissues that containendothelial cells and at least one of macrophages, osteoclasts orchondroclasts, with a composition comprising a biologically effectiveamount of at least a first VEGFR2-blocking, anti-VEGF antibody,optionally one that binds to substantially the same epitope as themonoclonal antibody 2C3 (ATCC PTA 1595), or an antigen-binding fragmentof the antibody, under conditions effective to inhibit VEGF-inducedangiogenesis and to treat an angiogenic disease without significantlyinhibiting VEGF stimulation of macrophages, osteoclasts orchondroclasts.

Methods of, and uses in, inhibiting VEGF-induced angiogenesis and,preferably, treating an anti-angiogenic disease, without causingsignificant side effects on bone metabolism are further provided. Themethods generally comprise contacting a tissue or a population ofangiogenic vessels that contain vascular endothelial cells and at leastone of macrophages, osteoclasts or chondroclasts, with a compositioncomprising a biologically effective amount of at least a firstVEGFR2-blocking, anti-VEGF antibody, optionally one that binds tosubstantially the same epitope as the monoclonal antibody 2C3 (ATCC PTA1595), or an antigen-binding fragment of the antibody, under conditionseffective to inhibit VEGF-induced angiogenesis and to treat anangiogenic disease without causing significant side effects on bonemetabolism by not significantly impairing the activities of macrophages,osteoclasts or chondroclasts.

Anti-angiogenic drug screening (in vitro) and therapy (in vivo) areprovided in terms of animals and patients that have, or are at risk fordeveloping, any disease or disorder characterized by undesired,inappropriate, aberrant, excessive and/or pathological vascularization.It is well known to those of ordinary skill in the art that as aberrantangiogenesis occurs in a wide range of diseases and disorders, a givenanti-angiogenic therapy, once shown to be effective in any acceptablemodel system, can be used to treat the entire range of diseases anddisorders connected with angiogenesis.

The methods and uses of the present invention are particularly intendedfor use in animals and patients that have, or are at risk fordeveloping, any form of vascularized tumor; macular degeneration,including age-related macular degeneration; arthritis, includingrheumatoid arthritis; atherosclerosis and atherosclerotic plaques;diabetic retinopathy and other retinopathies; thyroid hyperplasias,including Grave's disease; hemangioma; neovascular glaucoma; andpsoriasis.

The methods and uses of the invention are further intended for thetreatment of animals and patients that have, or are at risk fordeveloping, arteriovenous malformations (AVM), meningioma, and vascularrestenosis, including restenosis following angioplasty. Other intendedtargets of the therapeutic methods and uses are animals and patientsthat have, or are at risk for developing, angiofibroma, dermatitis,endometriosis, hemophilic joints, hypertrophic scars, inflammatorydiseases and disorders, pyogenic granuloma, scleroderma, synovitis,trachoma and vascular adhesions.

As disclosed in U.S. Pat. No. 5,712,291, specifically incorporatedherein by reference, each of the foregoing somewhat preferred treatmentgroups are by no means exhaustive of the types of conditions that are tobe treated by the present invention. U.S. Pat. No. 5,712,291 isincorporated herein by reference for certain specific purposes,including the purpose of identifying a number of other conditions thatmay be effectively treated by an anti-angiogenic therapeutic; thepurpose of showing that the treatment of all angiogenic diseasesrepresents a unified concept, once a defined category ofangiogenesis-inhibiting compounds have been disclosed and claimed (inthe present case, VEGFR2-blocking, anti-VEGF antibodies, optionallythose that bind to substantially the same epitope as the monoclonalantibody 2C3 (ATCC PTA 1595)); and the purpose of showing that thetreatment of all angiogenic diseases is enabled by data from only asingle model system.

In yet further aspects, and as disclosed in U.S. Pat. No. 5,712,291,incorporated herein by reference, the methods and uses of the presentinvention are intended for the treatment of animals and patients thathave, or are at risk for developing, abnormal proliferation offibrovascular tissue, acne rosacea, acquired immune deficiency syndrome,artery occlusion, atopic keratitis, bacterial ulcers, Bechets disease,blood borne tumors, carotid obstructive disease, chemical burns,choroidal neovascularization, chronic inflammation, chronic retinaldetachment, chronic uveitis, chronic vitritis, contact lens overwear,corneal graft rejection, corneal neovascularization, corneal graftneovascularization, Crohn's disease, Eales disease, epidemickeratoconjunctivitis, fungal ulcers, Herpes simplex infections, Herpeszoster infections, hyperviscosity syndromes, Kaposi's sarcoma, leukemia,lipid degeneration, Lyme's disease, marginal keratolysis, Mooren ulcer,Mycobacteria infections other than leprosy, myopia, ocular neovasculardisease, optic pits, Osler-Weber syndrome (Osler-Weber-Rendu,osteoarthritis, Pagets disease, pars planitis, pemphigoid,phylectenulosis, polyarteritis, post-laser complications, protozoaninfections, pseudoxanthoma elasticum, pterygium keratitis sicca, radialkeratotomy, retinal neovascularization, retinopathy of prematurity,retrolental fibroplasias, sarcoid, scleritis, sickle cell anemia,Sogrens syndrome, solid tumors, Stargarts disease, Steven's Johnsondisease, superior limbic keratitis, syphilis, systemic lupus, Terrien'smarginal degeneration, toxoplasmosis, trauma, tumors of Ewing sarcoma,tumors of neuroblastoma, tumors of osteosarcoma, tumors ofretinoblastoma, tumors of rhabdomyosarcoma, ulceritive colitis, veinocclusion, Vitamin A deficiency and Wegeners sarcoidosis.

The present invention further provides methods and uses for thetreatment of animals and patients that have, or are at risk fordeveloping, arthritis, in common with the treatment of arthritis usingimmunological agents described in U.S. Pat. No. 5,753,230, specificallyincorporated herein by reference. U.S. Pat. No. 5,972,922 is alsospecifically incorporated herein by reference to even further exemplifythe application of anti-angiogenic strategies to the treatment ofundesired angiogenesis associated with diabetes, parasitic diseases,abnormal wound healing, hypertrophy following surgery, bums, injury ortrauma, inhibition of hair growth, inhibition of ovulation and corpusluteum formation, inhibition of implantation and inhibition of embryodevelopment in the uterus. All of the foregoing conditions are thereforecontemplated for treatment by the methods and uses of the presentinvention.

U.S. Pat. No. 5,639,757 is further specifically incorporated herein byreference to exemplify the use of anti-angiogenic strategies to thegeneral treatment of graft rejection. The treatment of lunginflammation, nephrotic syndrome, preeclampsia, pericardial effusion,such as that associated with pericarditis, and pleural effusion usinganti-angiogenic strategies based upon VEGF inhibition is described in WO98/45331, specifically incorporated herein by reference. Animals andpatients that have, or are at risk for developing, any of the foregoingconditions are therefore contemplated for treatment by the methods anduses of the present invention.

As disclosed in WO 98/16551, specifically incorporated herein byreference, biological molecules that antagonize VEGF function are alsosuitable for use in treating diseases and disorders characterized byundesirable vascular permeability. Accordingly, the VEGF antagonizingantibodies, methods and uses of the present invention are applicable tothe treatment of animals and patients that have, or are at risk fordeveloping, diseases and disorders characterized by undesirable vascularpermeability, e.g., edema associated with brain tumors, ascitesassociated with malignancies, Meigs' syndrome, lung inflammation,nephrotic syndrome, pericardial effusion and pleural effusion and thelike.

Although the treatment of all the foregoing diseases is enabled withinthe present, unified invention, a particularly preferred aspect of themethods and uses of the present invention is application ofanti-angiogenic therapy to animals and patients that have, or are atrisk for developing, a vascularized solid tumor, a metastatic tumor ormetastases from a primary tumor.

Methods of, and uses in, inhibiting VEGF-induced angiogenesis, and,preferably, exerting an anti-tumor or improved anti-tumor effect withoutsignificantly inhibiting VEGF stimulation of macrophages, osteoclasts orchondroclasts are further provided. The methods generally comprisecontacting a tissue, tumor environment or population of angiogenicvessels that contain vascular endothelial cells and at least one ofmacrophages, osteoclasts or chondroclasts, with a composition comprisinga biologically effective amount of at least a first VEGFR2-blocking,anti-VEGF antibody, optionally one that binds to substantially the sameepitope as the monoclonal antibody 2C3 (ATCC PTA 1595), or anantigen-binding fragment of the antibody, under conditions effective toinhibit VEGF-induced angiogenesis and to exert an anti-tumor or improvedanti-tumor effect without significantly inhibiting VEGF stimulation ofmacrophages, osteoclasts or chondroclasts.

The present invention thus further provides methods of, and uses in,treating a disease associated with angiogenesis, including all forms ofcancer associated with angiogenesis, comprising administering to ananimal or patient with such a disease or cancer a therapeuticallyeffective amount of at least a first pharmaceutical composition thatcomprises a VEGFR2-blocking, anti-VEGF antibody, optionally one thatbinds to substantially the same epitope as the monoclonal antibody 2C3(ATCC PTA 1595), or an antigen-binding fragment or immnunoconjugate ofsuch an anti-VEGF antibody.

This invention links both anti-angiogenic methods using unconjugated ornaked antibodies and fragments thereof, and vascular targeting methodsusing immunoconjugates in which the antibody, or antigen-bindingfragment thereof, is operatively attached to a therapeutic agent. Unlessotherwise specifically stated or made clear in scientific terms, theterms “antibody and fragment thereof, as used herein, therefore mean an“unconjugated or naked” antibody or fragment, which is not attached toanother agent, particularly a therapeutic or diagnostic agent. Thesedefinitions do not exclude modifications of the antibody, such as, byway of example only, modifications to improve the biological half life,affinity, avidity or other properties of the antibody, or combinationsof the antibody with other effectors.

The anti-angiogenic treatment methods and uses of the invention alsoencompass the use of both unconjugated or naked antibodies andimmunoconjugates. In the immunoconjugate-based anti-angiogenic treatmentmethods, the antibody, or antigen-binding fragment thereof, ispreferably operatively attached to a second anti-angiogenic agent (theanti-VEGF antibody itself, being the first anti-angiogenic agent). Theattached anti-angiogenic agents may be those that have a direct orindirect anti-angiogenic effect.

The anti-angiogenic treatment methods and uses comprise administering toan animal or patient with a disease associated with angiogenesis,including all forms of cancer associated with angiogenesis, atherapeutically effective amount of at least a first pharmaceuticalcomposition that comprises at least a first unconjugated or nakedVEGFR2-blocking, anti-VEGF antibody, or antigen-binding fragmentthereof, optionally that binds to substantially the same epitope as themonoclonal antibody 2C3 (ATCC PTA 1595). Equally, the administeredantibody may be operatively associated with a second anti-angiogenicagent.

Methods for, and uses in, treating metastatic cancer compriseadministering to an animal or patient with metastatic cancer atherapeutically effective amount of at least a first pharmaceuticalcomposition that comprises at least a first an unconjugated or nakedVEGFR2-blocking, anti-VEGF antibody, or antigen-binding fragmentthereof, optionally one that binds to substantially the same epitope asthe monoclonal antibody 2C3 (ATCC PTA 1595). Further methods are thosewherein the administered antibody may be operatively associated with asecond anti-angiogenic agent.

Methods for, and uses in, reducing metastases from a primary cancercomprise administering a therapeutically effective amount of at least afirst unconjugated or naked VEGFR2-blocking, anti-VEGF antibody, orantigen-binding fragment thereof, to an animal or patient that has, orwas treated for, a primary cancer; wherein the unconjugated or nakedVEGFR2-blocking, anti-VEGF antibody or fragment thereof optionally bindsto substantially the same epitope as the monoclonal antibody 2C3 (ATCCPTA 1595). Similarly, the administered antibody may be operativelyassociated with a second anti-angiogenic agent.

Methods for, and uses in, treating a disease associated withangiogenesis, including all forms of cancer associated withangiogenesis, further comprise administering to an animal or patientwith such a disease, e.g., a vascularized tumor, at least a firstunconjugated or naked VEGFR2-blocking, anti-VEGF antibody, optionallyone that binds to substantially the same epitope as the monoclonalantibody 2C3 (ATCC PTA 1595), or an antigen-binding fragment thereof, inan amount effective to inhibit angiogenesis within the disease site orvascularized tumor. Equally, the administered antibody may beoperatively associated with a second anti-angiogenic agent.

The methods for, and uses in, treating a disease associated withangiogenesis, including all forms of cancer associated withangiogenesis, further comprise administering to an animal or patientwith such a disease or cancer at least a first unconjugated or nakedVEGFR2-blocking, anti-VEGF antibody, optionally one that binds tosubstantially the same epitope as the monoclonal antibody 2C3 (ATCC PTA1595), or an antigen-binding fragment thereof, in an amount effective toinhibit VEGF binding to the VEGF receptor VEGFR2 (KDR/Flk-1), therebyinhibiting angiogenesis within the disease or cancerous site. Theadministered antibody may alternatively be operatively associated with asecond anti-angiogenic agent.

Methods for, and uses in, treating a disease associated withangiogenesis, including all forms of cancer associated withangiogenesis, also comprise administering to an animal or patient with avascularized tumor a therapeutically effective amount of at least afirst unconjugated or naked VEGFR2-blocking, anti-VEGF antibody,optionally one that binds to substantially the same epitope as themonoclonal antibody 2C3 (ATCC PTA 1595), or antigen-binding fragmentthereof; wherein the anti-VEGF antibody substantially inhibits VEGFbinding to the VEGF receptor VEGFR2 (KDR/Flk-1) without significantlyinhibiting VEGF binding to the VEGF receptor VEGFR1 (Flt-1). Equally,the administered antibody may be operatively associated with a secondanti-angiogenic agent.

Yet further methods for, and uses in, treating a disease associated withangiogenesis, including all forms of cancer associated withangiogenesis, comprise administering to an animal or patient with such adisease, cancer or vascularized tumor a therapeutically effective amountof at least a first unconjugated or naked VEGFR2-blocking, anti-VEGFantibody, optionally one that binds to substantially the same epitope asthe monoclonal antibody 2C3 (ATCC PTA 1595), or an antigen-bindingfragment thereof; wherein the anti-VEGF antibody substantially inhibitsVEGF binding to the VEGF receptor VEGFR2 (KDR/Flk-1) withoutsignificantly inhibiting VEGF binding to the VEGF receptor VEGFR1(Flt-1), thereby inhibiting angiogenesis within the disease site, canceror vascularized tumor without significantly impairing macrophagechemotaxis in the animal. The administered antibody may also beoperatively associated with a second anti-angiogenic agent.

Still further methods for, and uses in, treating a disease associatedwith angiogenesis, including all forms of cancer associated withangiogenesis, comprise administering to an animal or patient with such adisease, cancer or vascularized tumor a therapeutically effective amountof at least a first unconjugated or naked VEGFR2-blocking, anti-VEGFantibody, optionally one that binds to substantially the same epitope asthe monoclonal antibody 2C3 (ATCC PTA 1595), or an antigen-bindingfragment thereof; wherein the anti-VEGF antibody substantially inhibitsVEGF binding to the VEGF receptor VEGFR2 (KDR/Flk-1) withoutsignificantly inhibiting VEGF binding to the VEGF receptor VEGFR1(Flt-1), thereby inhibiting angiogenesis within the disease site, canceror vascularized tumor without significantly impairing macrophage,osteoclast and/or chondroclast activity in the animal. Equally, theadministered antibody may be operatively associated with a secondanti-angiogenic agent.

Methods for, and uses in, treating a disease associated withangiogenesis, including all forms of cancer associated withangiogenesis, further comprise administering to an animal or patientwith such a disease, e.g., a vascularized tumor, at least a firstunconjugated or naked VEGFR2-blocking, anti-VEGF antibody, optionallyone that binds to substantially the same epitope as the monoclonalantibody 2C3 (ATCC PTA 1595), or an antigen-binding fragment thereof, inan amount effective to inhibit angiogenesis within the disease site orvascularized tumor without exerting a significant adverse on bonemetabolism.

The foregoing anti-angiogenic treatment methods and uses will generallyinvolve the administration of the pharmaceutically effective compositionto the animal or patient systemically, such as by transdermal,intramuscular, intravenous injection and the like. However, any route ofadministration that allows the therapeutic agent to localize to theangiogenic site or sites, including tumor or intratumoral vascularendothelial cells, will be acceptable. Therefore, other suitable routesof delivery include oral, rectal, nasal, topical, and vaginal. U.S. Pat.No. 5,712,291, is specifically incorporated herein by reference forpurposes including further describing the various routes ofadministration that may be included in connection with the treatment ofan angiogenic disease or disorder.

For uses and methods for the treatment of arthritis, e.g., intrasynovialadministration may be employed, as described for other immunologicalagents in U.S. Pat. No. 5,753,230, specifically incorporated herein byreference. For conditions associated with the eye, ophthalmicformulations and administration are contemplated.

“Administration”, as used herein, means provision or delivery ofVEGFR2-blocking, anti-VEGF antibody or 2C3-based therapeutics in anamount(s) and for a period of time(s) effective to exert anti-angiogenicand/or anti-tumor effects. The passive administration of proteinaceoustherapeutics is generally preferred, in part, for its simplicity andreproducibility.

However, the term “administration” is herein used to refer to any andall means by which VEGFR2-blocking, anti-VEGF antibody or 2C3-basedtherapeutics are delivered or otherwise provided to the tumorvasculature. “Administration” therefore includes the provision of cellsthat produce the VEGFR2-blocking, anti-VEGF antibody or 2C3-basedtherapeutics in a manner effective to result in delivery to the tumor.In such embodiments, it may be desirable to formulate or package thecells in a selectively permeable membrane, structure or implantabledevice, generally one that can be removed to cease therapy. ExogenousVEGFR2-blocking, anti-VEGF antibody or 2C3-like administration willstill generally be preferred, as this represents a non-invasive methodthat allows the dose to be closely monitored and controlled.

The therapeutic methods and uses of the invention also extend to theprovision of nucleic acids that encode VEGFR2-blocking, anti-VEGFantibody or 2C3-based therapeutics in a manner effective to result intheir expression in the vicinity of the tumor or their localization tothe tumor. Any gene therapy technique may be employed, such as naked DNAdelivery, recombinant genes and vectors, cell-based delivery, includingex vivo manipulation of patients' cells, and the like.

In yet further embodiments, the invention provides methods for, and usesin, delivering selected therapeutic or diagnostic agents to angiogenicblood vessels associated with disease. Such embodiments are preferablyused for delivering selected therapeutic or diagnostic agents to tumoror intratumoral vasculature or stroma, and comprise administering to ananimal or patient having a vascularized tumor a biologically effectiveamount of a composition comprising at least a first immunoconjugate inwhich a diagnostic or therapeutic agent is operatively attached to aVEGFR2-blocking, anti-VEGF antibody, or antigen-binding fragmentthereof, optionally one that binds to substantially the same epitope asthe monoclonal antibody 2C3 (ATCC PTA 1595).

Although understanding the mechanism of action underlying the targetingaspects of the invention is not required in order to practice suchembodiments, it is believed that the antibodies of the invention deliverattached agents to angiogenic and tumor vasculature by virtue of bindingto VEGF bound to the VEGFR1 expressed thereon. These methods and uses ofthe invention thus concern delivering selected therapeutic or diagnosticagents to angiogenic blood vessels, tumor or intratumoral vasculature,and comprise administering to an animal or patient in need of treatmenta biologically effective amount of a composition comprising animmunoconjugate in which a diagnostic or therapeutic agent isoperatively attached to at least a first VEGFR2-blocking, anti-VEGFantibody, or antigen-binding fragment thereof, optionally one that bindsto substantially the same epitope as the monoclonal antibody 2C3 (ATCCPTA 1595), in a manner effective to allow binding of the antibody toVEGF bound to VEGFR1 expressed, overexpressed or upregulated on theangiogenic blood vessels, tumor or intratumoral vasculature, thusdelivering the diagnostic or therapeutic agent to the VEGF-VEGFR1 on theangiogenic blood vessels, tumor or intratumoral vasculature.

The delivery of selected therapeutic agents to tumor or intratumoralvasculature or stroma acts to arrest blood flow, or specifically arrestblood flow, in tumor vasculature; to destroy, or specifically destroy,tumor vasculature; and to induce necrosis, or specific necrosis in atumor. These methods and uses may thus be summarized as methods fortreating an animal or patient having a vascularized tumor, comprisingadministering to the animal or patient a therapeutically effectiveamount of at least a first pharmaceutical composition comprising atleast a first immunoconjugate that comprises a VEGFR2-blocking,anti-VEGF antibody, optionally one that binds to substantially the sameepitope as the monoclonal antibody 2C3 (ATCC PTA 1595), orantigen-binding fragment thereof, operatively attached to a therapeuticagent.

The “therapeutically effective amounts” for use in the invention areamounts of VEGFR2-blocking, anti-VEGF antibody or 2C3-basedimmunoconjugates effective to specifically kill at least a portion oftumor or intratumoral vascular endothelial cells; to specifically induceapoptosis in at least a portion of tumor or intratumoral vascularendothelial cells; to specifically promote coagulation in at least aportion of tumor or intratumoral blood vessels; to specifically occludeor destroy at least a portion of blood transporting vessels of thetumor; to specifically induce necrosis in at least a portion of a tumor;and/or to induce tumor regression or remission upon administration toselected animals or patients. Such effects are achieved while exhibitinglittle or no binding to, or little or no killing of, vascularendothelial cells in normal, healthy tissues; little or no coagulationin, occlusion or destruction of blood vessels in healthy, normaltissues; and exerting negligible or manageable adverse side effects onnormal, healthy tissues of the animal or patient.

The terms “preferentially” and “specifically”, as used herein in thecontext of promoting coagulation in, or destroying, tumor vasculature,and/or in the context of binding to tumor stroma and/or causing tumornecrosis, thus mean that the VEGFR2-blocking, anti-VEGF antibody or2C3-based immunoconjugates function to achieve stromal binding,coagulation, destruction and/or tumor necrosis that is substantiallyconfined to the tumor stroma, vasculature and tumor site, and does notsubstantially extend to causing coagulation, destruction and/or tissuenecrosis in normal, healthy tissues of the animal or subject. Thestructure and function of healthy cells and tissues is thereforemaintained substantially unimpaired by the practice of the invention.

Although the antibodies of the invention effectively deliver agents toangiogenic and tumor vasculature by binding to VEGF in association withVEGFR1, other methods and uses operate on the basis of delivering atherapeutic agent to tumor stroma, wherein it exerts a therapeuticeffect on the nearby vessels. These methods and uses compriseadministering to an animal or patient with a vascularized tumor animmunoconjugate that comprises a therapeutic agent operatively attachedto at least a first VEGFR2-blocking, anti-VEGF antibody, orantigen-binding fragment thereof, optionally one that binds tosubstantially the same epitope as the monoclonal antibody 2C3 (ATCC PTA1595) in an amount effective to bind the immunoconjugate to non-receptorbound VEGF within the tumor stroma.

These methods and uses comprise administering to an animal or patientwith a vascularized tumor an immunoconjugate that comprises atherapeutic agent operatively attached to at least a firstVEGFR2-blocking, anti-VEGF antibody, or antigen-binding fragmentthereof, optionally one that binds to substantially the same epitope asthe monoclonal antibody 2C3 (ATCC PTA 1595) in an amount effective tolocalize the immunoconjugate within the tumor stroma such that theattached therapeutic agent exerts an anti-tumor effect on thesurrounding tumor vasculature and/or tumor cells.

The compositions, as well as the methods and uses, of the invention thusextend to compositions comprising VEGFR2-blocking, anti-VEGF antibody or2C3-based immunoconjugates comprising at least a first VEGFR2-blocking,anti-VEGF antibody, or antigen-binding fragment thereof, optionally onethat binds to substantially the same epitope as the monoclonal antibody2C3 (ATCC PTA 1595), operatively attached to at least a firsttherapeutic or diagnostic agent. VEGFR2-blocking, anti-VEGF antibody or2C3-based therapeutic conjugates are preferably linked toradiotherapeutic agents, anti-angiogenic agents, apoptosis-inducingagents, anti-tubulin drugs, anti-cellular or cytotoxic agents, orcoagulants (coagulation factors).

The invention thus provides a range of conjugated antibodies andfragments thereof in which the antibody is operatively attached to atleast a first therapeutic or diagnostic agent. The term“immunoconjugate” is broadly used to define the operative association ofthe antibody with another effective agent and is not intended to refersolely to any type of operative association, and is particularly notlimited to chemical “conjugation”. Recombinant fusion proteins areparticularly contemplated. So long as the delivery or targeting agent isable to bind to the target and the therapeutic or diagnostic agent issufficiently functional upon delivery, the mode of attachment will besuitable.

Attachment of agents via the carbohydrate moieties on antibodies is alsocontemplated. Glycosylation, both O-linked and N-linked, naturallyoccurs in antibodies. Recombinant antibodies can be modified to recreateor create additional glycosylation sites if desired, which is simplyachieved by engineering the appropriate amino acid sequences (such asAsn-X-Ser, Asn-X-Thr, Ser, or Thr) into the primary sequence of theantibody.

Currently preferred agents for use in VEGFR2-blocking, anti-VEGFantibody or 2C3-based therapeutic conjugates and related methods anduses are those that complement or enhance the effects of the antibodyand/or those selected for a particular tumor type or patient.“Therapeutic agents that complement or enhance the effects of theantibody” include radiotherapeutic agents, anti-angiogenic agents,apoptosis-inducing agents and anti-tubulin rugs, any one or more ofwhich are preferred for use herewith.

The attachment or association of the preferred agents withVEGFR2-blocking. anti-VEGF or 2C3-based antibodies gives“immunoconjugates”, wherein such immunoconjugates often have enhancedand even synergistic anti-tumor properties. Currently preferredanti-angiogenic agents for use in this manner are angiostatin,endostatin, any one of the angiopoietins, vasculostatin, canstatin andmaspin. Currently preferred anti-tubulin drugs include colchicine,taxol, vinblastine, vincristine, vindescine and one or more of thecombretastatins.

The use of anti-cellular and cytotoxic agents results inVEGFR2-blocking, anti-VEGF antibody or 2C3-based “immunotoxins”, whereasthe use of coagulation factors results in VEGFR2-blocking, anti-VEGFantibody or 2C3-based “coaguligands”. The use of at least twotherapeutic agents is also contemplated, such as combinations of one ormore radiotherapeutic agents, anti-angiogenic agents, apoptosis-inducingagents, anti-tubulin drugs, anti-cellular and cytotoxic agents andcoagulation factors.

In certain applications, the VEGFR2-blocking, anti-VEGF antibody or2C3-based therapeutics will be operatively attached to cytotoxic,cytostatic or otherwise anti-cellular agents that have the ability tokill or suppress the growth or cell division of endothelial cells.Suitable anti-cellular agents include chemotherapeutic agents, as wellas cytotoxins and cytostatic agents. Cytostatic agents are generallythose that disturb the natural cell cycle of a target cell, preferablyso that the cell is taken out of the cell cycle.

Exemplary chemotherapeutic agents include: steroids; cytokines;anti-metabolites, such as cytosine arabinoside, fluorouracil,methotrexate or aminopterin; anthracyclines; mitomycin C; vincaalkaloids; antibiotics; demecolcine; etoposide; mithramycin; andanti-tumor alkylating agents, such as chlorambucil or melphalan. Indeed,any of the agents disclosed herein in Table C could be used. Certainpreferred anti-cellular agents are DNA synthesis inhibitors, such asdaunorubicin, doxorubicin, adriamycin, and the like.

In certain therapeutic applications, toxin moieties will be preferred,due to the much greater ability of most toxins to deliver a cell killingeffect, as compared to other potential agents. Therefore, certainpreferred anti-cellular agents for VEGFR2-blocking, anti-VEGF antibodyor 2C3-based antibody constructs are plant-, fungus- or bacteria-derivedtoxins. Exemplary toxins include epipodophyllotoxins; bacterialendotoxin or the lipid A moiety of bacterial endotoxin; ribosomeinactivating proteins, such as saporin or gelonin; a-sarcin;aspergillin; restrictocin; ribonucleases, such as placentalribonuclease; diphtheria toxin and pseudomonas exotoxin.

Preferred toxins are the A chain toxins, such as ricin A chain. The mostpreferred toxin moiety is often ricin A chain that has been treated tomodify or remove carbohydrate residues, so called “deglycosylated Achain” (dgA). Deglycosylated ricin A chain is preferred because of itsextreme potency, longer half-life, and because it is economicallyfeasible to manufacture it a clinical grade and scale. Recombinantand/or truncated ricin A chain may also be used.

For tumor targeting and treatment with immunotoxins, the followingpatents and patent applications are specifically incorporated herein byreference for the purposes of even further supplementing the presentteachings regarding anti-cellular and cytotoxic agents: U.S.applications Ser. Nos. 07/846,349; 08/295,868 (U.S. Pat. No. 6,004,554);Ser. No. 08/205,330 (U.S. Pat. No. 5,855,866); Ser. No. 08/350,212 (U.S.Pat. No. 5,965,132); Ser. No. 08/456,495 (U.S. Pat. No. 5,776,427); Ser.No. 08/457,487 (U.S. Pat. No. 5,863,538); Ser. Nos. 08/457,229 and08/457,031 (U.S. Pat. No. 5,660,827) and Ser. No. 08/457,869 (U.S. Pat.No. 6,051,230).

The 2C3-based or other VEGFR2-blocking, anti-VEGF antibody of thepresent invention may be linked to an anti-tubulin drug. “Anti-tubulindrug(s)”, as used herein, means any agent, drug, prodrug or combinationthereof that inhibits cell mitosis, preferably by directly or indirectlyinhibiting tubulin activities necessary for cell mitosis, preferablytubulin polymerization or depolymerization.

Currently preferred anti-tubulin drugs for use herewith are colchicine;taxanes. such as taxol; vinca alkaloids, such as vinblastine,vincristine and vindescine; and combretastatins. Exemplarycombretastatins are combretastatin A, B and/or D, including A-1, A-2,A-3, A-4, A-5, A-6, B-1, B-2, B-3, B-4, D-1 and D-2 and prodrug formsthereof.

The VEGFR2-blocking, anti-VEGF antibody or 2C3-based therapeutics maycomprise a component that is capable of promoting coagulation, i.e., acoagulant. Here, the targeting antibody may be directly or indirectly,e.g., via another antibody, linked to a factor that directly orindirectly stimulates coagulation.

Preferred coagulation factors for such uses are Tissue Factor (TF) andTF derivatives, such as truncated TF (tTF), dimeric, trimeric,polymeric/multimeric TF, and mutant TF deficient in the ability toactivate Factor VII. Other suitable coagulation factors include vitaminK-dependent coagulants, such as Factor II/IIa, Factor VII/VIIa, FactorIX/IXa and Factor X/Xa; vitamin K-dependent coagulation factors thatlack the Gla modification; Russell's viper venom Factor X activator;platelet-activating compounds, such as thromboxane A₂ and thromboxane A₂synthase; and inhibitors of fibrinolysis, such as α2-antiplasmin.

Tumor targeting and treatment with coaguligands is described in thefollowing patents and patent applications, each of which arespecifically incorporated herein by reference for the purposes of evenfurther supplementing the present teachings regarding coaguligands andcoagulation factors: U.S. applications Ser. Nos. 07/846,349; 08/205,330(U.S. Pat. No. 5,855,866); Ser. No. 08/350,212 (U.S. Pat. No.5,965,132); Ser. Nos. 08/273,567; 08/482,369 (U.S. Pat. No. 6,093,399)Oct. 20, 1998); Ser. Nos. 08/485,482; 08/487,427 (U.S. Pat. No.6,004,555); Ser. No. 08/479,733 (U.S. Pat. No. 5,877,289); Ser. Nos.08/472,631; and 08/479,727 and 08/481,904 (U.S. Pat. No. 6,036,955).

The preparation of immunoconjugates and immunotoxins is generally wellknown in the art (see, e.g., U.S. Pat. No. 4,340,535, incorporatedherein by reference). Each of the following patents and patentapplications are further incorporated herein by reference for thepurposes of even further supplementing the present teachings regardingimmunotoxin generation, purification and use: U.S. applications Ser.Nos. 07/846,349; 08/295,868 (U.S. Pat. No. 6,004,554); Ser. No.08/205,330 (U.S. Pat. No. 5,855,866); Ser. No. 08/350,212 (U.S. Pat. No.5,965,132); Ser. No. 08/456,495 (U.S. Pat. No. 5,776,427); Ser. No.08/457,487 (U.S. Pat. No. 5,863,538); Ser. Nos. 08/457,229 and08/457,031 (U.S. Pat. No. 5,660,827) and Ser. No. 08/457,869 (U.S. Pat.No. 6,051,230).

In the preparation of immunoconjugates and immunotoxins, advantages maybe achieved through the use of certain linkers. For example, linkersthat contain a disulfide bond that is sterically “hindered” are oftenpreferred, due to their greater stability in vivo, thus preventingrelease of the toxin moiety prior to binding at the site of action. Itis generally desired to have a conjugate that will remain intact underconditions found everywhere in the body except the intended site ofaction, at which point it is desirable that the conjugate have good“release” characteristics.

Depending on the specific toxin compound used, it may be necessary toprovide a peptide spacer operatively attaching the VEGFR2-blocking,anti-VEGF antibody or 2C3-based antibody and the toxin compound, whereinthe peptide spacer is capable of folding into a disulfide-bonded loopstructure. Proteolytic cleavage within the loop would then yield aheterodimeric polypeptide wherein the antibody and the toxin compoundare linked by only a single disulfide bond.

When certain other toxin compounds are utilized, a non-cleavable peptidespacer may be provided to operatively attach the VEGFR2-blocking,anti-VEGF antibody or 2C3-based antibody and the toxin compound. Toxinsthat may be used in conjunction with non-cleavable peptide spacers arethose that may, themselves, be converted by proteolytic cleavage, into acytotoxic disulfide-bonded form. An example of such a toxin compound isa Pseudonomas exotoxin compound.

A variety of chemotherapeutic and other pharmacological agents can alsobe successfully conjugated to VEGFR2-blocking, anti-VEGF antibody or2C3-based therapeutics. Exemplary antineoplastic agents that have beenconjugated to antibodies include doxorubicin, daunomycin, methotrexateand vinblastine. Moreover, the attachment of other agents such asneocarzinostatin, macromycin, trenimon and α-amanitin has been described(see U.S. Pat. Nos. 5,660,827; 5,855,866; and 5,965,132; eachincorporated herein.)

In light of one of the present inventors earlier work, the preparationof coaguligands is now also easily practiced. The operable associationof one or more coagulation factors with a VEGFR2-blocking, anti-VEGFantibody or 2C3-based antibody may be a direct linkage, such as thosedescribed above for the immunotoxins. Alternatively, the operativeassociation may be an indirect attachment, such as where the antibody isoperatively attached to a second binding region, preferably an antibodyor antigen binding region of an antibody, that binds to the coagulationfactor. The coagulation factor should be attached to theVEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody at a sitedistinct from its functional coagulating site, particularly where acovalent linkage is used to join the molecules.

Indirectly linked coaguligands are often based upon bispecificantibodies. The preparation of bispecific antibodies is also well knownin the art. One preparative method involves the separate preparation ofantibodies having specificity for the targeted tumor component, on theone hand, and the coagulating agent on the other. Peptic F(ab′γ)₂fragments from the two chosen antibodies are then generated, followed byreduction of each to provide separate Fab′γSH fragments. The SH groupson one of the two partners to be coupled are then alkylated with across-linking reagent, such as o-phenylenedimaleimide, to provide freemaleimide groups on one partner. This partner may then be conjugated tothe other by means of a thioether linkage, to give the desired F(ab′γ)₂heteroconjugate (Glennie et al., 1987; incorporated herein byreference). Other approaches, such as cross-linking with SPDP or proteinA may also be carried out.

Another method for producing bispecific antibodies is by the fusion oftwo hybridomas to form a quadroma. As used herein, the term “quadroma”is used to describe the productive fusion of two B cell hybridomas.Using now standard techniques, two antibody producing hybridomas arefused to give daughter cells, and those cells that have maintained theexpression of both sets of clonotype immunoglobulin genes are thenselected.

A preferred method of generating a quadroma involves the selection of anenzyme deficient mutant of at least one of the parental hybridomas. Thisfirst mutant hybridoma cell line is then fused to cells of a secondhybridoma that had been lethally exposed, e.g., to iodoacetamide,precluding its continued survival. Cell fusion allows for the rescue ofthe first hybridoma by acquiring the gene for its enzyme deficiency fromthe lethally treated hybridoma, and the rescue of the second hybridomathrough fusion to the first hybridoma. Preferred, but not required, isthe fusion of immunoglobulins of the same isotype, but of a differentsubclass. A mixed subclass antibody permits the use if an alternativeassay for the isolation of a preferred quadroma.

Microtiter identification embodiments, FACS, immunofluorescencestaining, idiotype specific antibodies, antigen binding competitionassays, and other methods common in the art of antibody characterizationmay be used to identify preferred quadromas. Following the isolation ofthe quadroma, the bispecific antibodies are purified away from othercell products. This may be accomplished by a variety of antibodyisolation procedures, known to those skilled in the art ofimmunoglobulin purification (see, e.g., Antibodies: A Laboratory Manual,1988; incorporated herein by reference). Protein A or protein Gsepharose columns are preferred.

In the preparation of immunoconjugates, immunotoxins and coaguligands,recombinant expression may be employed. The nucleic acid sequencesencoding the chosen VEGFR2-blocking, anti-VEGF antibody or 2C3-basedantibody, and therapeutic agent, toxin or coagulant, are attachedin-frame in an expression vector. Recombinant expression thus results intranslation of the nucleic acid to yield the desired immunoconjugate.Chemical cross-linkers and avidin:biotin bridges may also join thetherapeutic agents to the VEGFR2-blocking, anti-VEGF antibody or2C3-based antibodies.

The following patents and patent applications are each incorporatedherein by reference for the purposes of even further supplementing thepresent teachings regarding coaguligand preparation, purification anduse, including bispecific antibody coaguligands: U.S. applications Ser.Nos. 07/846,349; 08/205,330 (U.S. Pat. No. 5,855,866); Ser. No.08/350,212 (U.S. Pat. No. 5,965,132); Ser. Nos. 08/273,567; 08/482,369(U.S. Pat. No. 6,093,099; Oct. 20, 1998); Ser. Nos. 08/485,482;08/487,427 (U.S. Pat. No. 6,004,555); Ser. No. 08/479,733 (U.S. Pat. No.5,877,289); Ser. Nos. 08/472,631; and 08/479,727 and 08/481,904 (U.S.Pat. No. 6,036,955).

Immunoconjugates with radiotherapeutic agents, anti-angiogenic agents,apoptosis-inducing agents, anti-tubulin drugs, toxins and coagulants,whether prepared by chemical conjugation or recombinant expression, mayemploy a biologically-releasable bond and/or a selectively cleavablespacer or linker. Such compositions are preferably reasonably stableduring circulation and are preferentially or specifically released upondelivery to the disease or tumor site.

Certain preferred examples are acid sensitive spacers, whereinVEGFR2-blocking, anti-VEGF antibodies linked to colchicine ordoxorubicin are particularly contemplated. Other preferred examples arepeptide linkers that include a cleavage site for peptidases and/orproteinases that are specifically or preferentially present or activewithin a disease site. such as a tumor environment. The delivery of theimmunoconjugate to the disease or tumor site results in cleavage and therelatively specific release of the coagulation factor.

Peptide linkers that include a cleavage site for urokinase,pro-urokinase, plasmin, plasminogen, TGFβ, staphylokinase, Thrombin,Factor IXa, Factor Xa or a metalloproteinase (MMP), such as aninterstitial collagenase, a gelatinase or a stromelysin, areparticularly preferred, as described and enabled by U.S. Pat. No.5,877,289, incorporated herein by reference for such purposes, andfurther exemplified herein in Table B2.

The VEGFR2-blocking, anti-VEGF antibody may also be derivatized tointroduce functional groups permitting the attachment of the therapeuticagent(s) through a biologically releasable bond. The targeting antibodymay thus be derivatized to introduce side chains terminating inhydrazide, hydrazine, primary amine or secondary amine groups.Therapeutic agents may be conjugated through a Schiff's base linkage, ahydrazone or acyl hydrazone bond or a hydrazide linker (U.S. Pat. Nos.5,474,765 and 5,762,918, each specifically incorporated herein byreference).

Whether primarily anti-angiogenic or vascular-targeting based, thecompositions and methods of the present invention may be used incombination with other therapeutics and diagnostics. In terms ofbiological agents, preferably diagnostic or therapeutic agents. for use“in combination” with a VEGFR2-blocking, anti-VEGF antibody inaccordance with the present invention, such as a 2C3-based antibody, theterm “in combination” is succinctly used to cover a range ofembodiments. The “in combination” terminology, unless otherwisespecifically stated or made clear from the scientific terminology, thusapplies to various formats of combined compositions, pharmaceuticals,cocktails, kits, methods, and first and second medical uses.

The “combined” embodiments of the invention thus include, for example,where the VEGFR2-blocking, anti-VEGF or 2C3-based antibody is a nakedantibody and is used in combination with an agent or therapeutic agentthat is not operatively attached thereto. In such cases, the agent ortherapeutic agent may be used in a non-targeted or targeted form. In“non-targeted form”, the agent, particularly therapeutic agents, willgenerally be used according to their standard use in the art. In“targeted form”, the agent will generally be operatively attached to adistinct antibody or targeting region that delivers the agent ortherapeutic agent to the angiogenic disease site or tumor. The use ofsuch targeted forms of biological agents, both diagnostics andtherapeutics, is also quite standard in the art.

In other “combined” embodiments of the invention, the VEGFR2-blocking,anti-VEGF or 2C3-based antibody is an immunoconjugate wherein theantibody is itself operatively associated or combined with the agent ortherapeutic agent. In certain preferred examples, the agent, includingdiagnostic and therapeutic agents, will be a “2C3-targeted agent”. Theoperative attachment includes all forms of direct and indirectattachment as described herein and known in the art.

The “combined” uses, particularly in terms of VEGFR2-blocking, anti-VEGFor 2C3-based antibodies in combination with therapeutic agents, alsoinclude combined compositions, pharmaceuticals, cocktails, kits,methods, and first and second medical uses wherein the therapeutic agentis in the form of a prodrug. In such embodiments, the activatingcomponent able to convert the prodrug to the functional form of the drugmay again be operatively associated with the VEGFR2-blocking, anti-VEGFor 2C3-based antibodies of the present invention.

In certain preferred embodiments, the therapeutic compositions,combinations, pharmaceuticals, cocktails, kits, methods, and first andsecond medical uses will be “2C3-prodrug combinations”. As will beunderstood by those of ordinary skill in the art, the term “2C3-prodrugcombination”, unless otherwise stated, means that the 2C3-based antibodyis operatively attached to a component capable of converting the prodrugto the active drug, not that the 2C3 -based antibody is attached to theprodrug itself However, there is no requirement that the prodrugembodiments of the invention need to be used as 2C3-prodrugcombinations. Accordingly, prodrugs may be used in any manner that theyare used in the art, including in ADEPT and other forms.

Thus, where combined compositions, pharmaceuticals, cocktails, kits,methods,. and first and second medical uses are described, preferably interms of diagnostic agents, and more preferably therapeutic agents, thecombinations include VEGFR2-blocking, anti-VEGF antibodies, such as2C3-based antibodies, that are naked antibodies and immunoconjugates,and wherein practice of the in vivo embodiments of the inventioninvolves the prior, simultaneous or subsequent administration of thenaked antibodies or immunoconjugate and the biological, diagnostic ortherapeutic agent; so long as, in some conjugated or unconjugated form,the overall provision of some form of the antibody and some form of thebiological, diagnostic or therapeutic agent is achieved.

Particularly preferred combined compositions, methods and uses of theinvention are those including VEGFR2-blocking, anti-VEGF antibodies andendostatin (U.S. Pat. No. 5,854,205, specifically incorporated herein byreference). These include where the VEGFR2-blocking, anti-VEGF antibodyor 2C3 construct is a naked antibody or immunoconjugate; and when animmunoconjugate, wherein the VEGFR2-blocking, anti-VEGF antibody or 2C3is linked to endostatin, optionally with angiostatin; wherein thecombined therapeutic method or use involves the prior, simultaneous, orsubsequent administration of endostatin, optionally with angiostatin; solong as, in some conjugated or unconjugated form, the overall provisionof 2C3, endostatin and optionally angiostatin is achieved.VEGFR2-blocking, anti-VEGF or 2C3-based antibodies operativelyassociated with collagenase are also provided, as the collagenase, whenspecifically delivered to the tumor, will produce endostatin in situ,achieving similar benefits.

The foregoing and other explanations of the effects of the presentinvention on tumors are made for simplicity to explain the combined modeof operation, type of attached agent(s) and such like. This descriptiveapproach should not be interpreted as either an understatement or anoversimplification of the beneficial properties of the VEGFR2-blocking,anti-VEGF antibodies or 2C3-based antibodies of the invention. It willtherefore be understood that such antibodies themselves haveanti-angiogenic properties and VEGF neutralization properties (such asneutralizing the survival function of VEGF), that immunoconjugates ofsuch antibodies will maintain these properties and combine them with theproperties of the attached agent; and further, that the combined effectof the antibody and any attached agent will typically be enhanced and/ormagnified.

The invention therefore provides compositions, pharmaceuticalcompositions, therapeutic kits and medicinal cocktails comprising,optionally in at least a first composition or container, a biologicallyeffective amount of at least a first VEGFR2-blocking, anti-VEGFantibody, optionally one that binds to substantially the same epitope asthe monoclonal antibody 2C3 (ATCC PTA 1595), or an antigen-bindingfragment or immunoconjugate of such an anti-VEGF antibody; and abiologically effective amount of at least a second biological agent,component or system.

The “at least a second biological agent, component or system” will oftenbe a therapeutic or diagnostic agent, component or system, but it notbe. For example, the at least a second biological agent, component orsystem may comprise components for modification of the antibody and/orfor attaching other agents to the antibody. Certain preferred secondbiological agents, components or systems are prodrugs or components formaking and using prodrugs, including components for making the prodrugitself and components for adapting the antibodies of the invention tofunction in such prodrug or ADEPT embodiments.

Where therapeutic or diagnostic agents are included as the at least asecond biological agent, component or system, such therapeutics and/ordiagnostics will typically be those for use in connection withangiogenic diseases. Such agents are those suitable for use in treatingor diagnosing a disease or disorder as disclosed in any one of U.S. Pat.Nos. 5,712,291, 5,753,230, 5,972,922, 5,639,757, WO 98/45331 and WO98/16551, each specifically incorporated herein by reference.

Where the disease to be treated is cancer, “at least a secondanti-cancer agent” will be included in the therapeutic kit or cocktail.The term “at least a second anti-cancer agent” is chosen in reference tothe VEGFR2-blocking, anti-VEGF antibody or 2C3 construct being the firstanti-cancer agent. The antibodies of the invention may thus be combinedwith chemotherapeutic agents, radiotherapeutic agents, cytokines,anti-angiogenic agents, apoptosis-inducing agents or anti-cancerimmunotoxins or coaguligands.

“Chemotherapeutic agents”, as used herein, refer to classicalchemotherapeutic agents or drugs used in the treatment of malignancies.This term is used for simplicity notwithstanding the fact that othercompounds may be technically described as chemotherapeutic agents inthat they exert an anti-cancer effect. However, “chemotherapeutic” hascome to have a distinct meaning in the art and is being used accordingto this standard meaning. A number of exemplary chemotherapeutic agentsare described herein. Those of ordinary skill in the art will readilyunderstand the uses and appropriate doses of chemotherapeutic agents,although the doses may well be reduced when used in combination with thepresent invention.

A new class of drugs that may also be termed “chemotherapeutic agents”are agents that induce apoptosis. Any one or more of such drugs,including genes, vectors, antisense constructs and ribozymes, asappropriate, may also be used in conjunction with the present invention.Currently preferred second agents are anti-angiogenic agents, such asangiostatin, endostatin, vasculostatin, canstatin and maspin.

Other exemplary anti-cancer agent include, e.g., neomycin,podophyllotoxin(s), TNF-α, α_(v),β₃ antagonists, calcium ionophores,calcium-flux inducing agents, and any derivative or prodrug thereof.Currently preferred anti-tubulin drugs include colchicine, taxol,vinblastine, vincristine, vindescine, a combretastatin or a derivativeor prodrug thereof.

Anti-cancer immunotoxins or coaguligands are further appropriateanti-cancer agents. “Anti-cancer immunotoxins or coaguligands”, ortargeting-agent/therapeutic agent constructs, are based upon targetingagents, including antibodies or antigen binding fragments thereof, thatbind to a targetable or accessible component of a tumor cell, tumorvasculature or tumor stroma, and that are operatively attached to atherapeutic agent, including cytotoxic agents (immunotoxins) andcoagulation factors (coaguligands). A “targetable or accessiblecomponent” of a tumor cell, tumor vasculature or tumor stroma, ispreferably a surface-expressed, surface-accessible or surface-localizedcomponent, although components released from necrotic or otherwisedamaged tumor cells or vascular endothelial cells may also be targeted,including cytosolic and/or nuclear tumor cell antigens.

Both antibody and non-antibody targeting agents may be used, includinggrowth factors, such as VEGF and FGF; peptides containing the tripeptideR-G-D, that bind specifically to the tumor vasculature; and othertargeting components such as annexins and related ligands.

Anti-tumor cell immunotoxins or coaguligands may comprise antibodiesexemplified by the group consisting of antibodies termed B3 (ATCC HB10573), 260F9 (ATCC HB 8488), D612 (ATCC HB 9796) and KS1/4, said KS1/4antibody obtained from a cell comprising the vector pGKC2310 (NRRLB-18356) or the vector pG2A52 (NRRL B-18357).

Anti-tumor cell targeting agents that comprise an antibody, or anantigen-binding region thereof, that binds to an intracellular componentthat is released from a necrotic tumor cell are also contemplated.Preferably such antibodies are monoclonal antibodies, or antigen-bindingfragments thereof, that bind to insoluble intracellular antigen(s)present in cells that may be induced to be permeable, or in cell ghostsof substantially all neoplastic and normal cells, but are not present oraccessible on the exterior of normal living cells of a mammal.

U.S. Pat. Nos. 5,019,368, 4,861,581 and 5,882,626, each issued to AlanEpstein and colleagues, are each specifically incorporated herein byreference for purposes of even further describing and teaching how tomake and use antibodies specific for intracellular antigens that becomeaccessible from malignant cells in vivo. The antibodies described aresufficiently specific to internal cellular components of mammalianmalignant cells, but not to external cellular components. Exemplarytargets include histones, but all intracellular components specificallyreleased from necrotic tumor cells are encompassed.

Upon administration to an animal or patient with a vascularized tumor,such antibodies localize to the malignant cells by virtue of the factthat vascularized tumors naturally contain necrotic tumor cells, due tothe process(es) of tumor re-modeling that occur in vivo and cause atleast a proportion of malignant cells to become necrotic. In addition,the use of such antibodies in combination with other therapies thatenhance tumor necrosis serves to enhance the effectiveness of targetingand subsequent therapy.

These types of antibodies may thus be used to directly or indirectlyassociate with angiopoietins and to administer the angiopoietins tonecrotic malignant cells within vascularized tumors, as genericallydisclosed herein.

As also disclosed in U.S. Pat. Nos. 5,019,368, 4,861,581 and 5,882,626,each incorporated herein by reference, these antibodies may be used incombined diagnostic methods (see below) and in methods for measuring theeffectiveness of anti-tumor therapies. Such methods generally involvethe preparation and administration of a labeled version of theantibodies and measuring the binding of the labeled antibody to theinternal cellular component target preferentially bound within necrotictissue. The methods thereby image the necrotic tissue, wherein alocalized concentration of the antibody is indicative of the presence ofa tumor and indicate ghosts of cells that have been killed by theanti-tumor therapy.

Anti-tumor stroma immunotoxins or coaguligands will generally compriseantibodies that bind to a connective tissue component, a basementmembrane component or an activated platelet component; as exemplified bybinding to fibrin, RIBS or LIBS.

Anti-tumor vasculature immunotoxins or coaguligands may compriseligands, antibodies, or fragments thereof, that bind to asurface-expressed, surface-accessible or surface-localized component ofthe blood transporting vessels, preferably the intratumoral bloodvessels, of a vascularized tumor. Such antibodies include those thatbind to surface-expressed components of intratumoral blood vessels of avascularized tumor, including intratumoral vasculature cell surfacereceptors, such as endoglin (TEC-4 and TEC-11antibodies), a TGFβreceptor, E-selectin, P-selectin, VCAM-1, ICAM-1, PSMA, a VEGF/VPFreceptor, an FGF receptor, a TIE, α_(v)β₃ integrin, pleiotropin,endosialin and MHC Class II proteins. The antibodies may also bind tocytokine-inducible or coagulant-inducible components of intratumoralblood vessels. Certain preferred agents will bind toamninophospholipids, such as phosphatidylserine orphosphatidylethanolamine.

Other anti-tumor vasculature immunotoxins or coaguligands may compriseantibodies, or fragments thereof, that bind to a ligand or growth factorthat binds to an intratumoral vasculature cell surface receptor. Suchantibodies include those that bind to VEGF/VPF (GV39 and GV97antibodies), FGF, TGFβ, a ligand that binds to a TIE, a tumor-associatedfibronectin isoform, scatter factor/hepatocyte growth factor (HGF),platelet factor 4 (PF4), PDGF and TIMP. The antibodies, or fragmentsthereof, may also bind to a ligand:receptor complex or a growthfactor:receptor complex, but not to the ligand or growth factor, or tothe receptor, when the ligand or growth factor or the receptor is not inthe ligand:receptor or growth factor:receptor complex.

Anti-tumor cell, anti-tumor stroma or anti-tumor vasculatureantibody-therapeutic agent constructs may comprise anti-angiogenicagents, apoptosis-inducing agents, anti-tubulin drugs, cytotoxic agentssuch as plant-, fungus- or bacteria-derived toxins. Ricin A chain anddeglycosylated ricin A chain will often be preferred. Anti-tumor cell,anti-tumor stroma or anti-tumor vasculature antibody-therapeutic agentconstructs may comprise coagulants (direct and indirect actingcoagulation factors) or second antibody binding regions that bind tocoagulation factors. The operative association with Tissue Factor orTissue Factor derivatives, such as truncated Tissue Factor, will oftenbe preferred.

In terms of compositions, kits and/or medicaments of the invention, thecombined effective amounts of the therapeutic agents may be comprisedwithin a single container or container means, or comprised withindistinct containers or container means. The cocktails will generally beadmixed together for combined use. Agents formulated for intravenousadministration will often be preferred. Imaging components may also beincluded. The kits may also comprise instructions for using the at leasta first antibody and the one or more other biological agents included.

Speaking generally, the at least a second anti-cancer agent may beadministered to the animal or patient substantially simultaneously withthe VEGFR2-blocking, anti-VEGF antibody or 2C3-based therapeutic; suchas from a single pharmaceutical composition or from two pharmaceuticalcompositions administered closely together.

Alternatively, the at least a second anti-cancer agent may beadministered to the animal or patient at a time sequential to theadministration of the VEGFR2-blocking, anti-VEGF antibody or 2C3-basedtherapeutic. “At a time sequential”, as used herein, means “staggered”,such that the at least a second anti-cancer agent is administered to theanimal or patient at a time distinct to the administration of theVEGFR2-blocking, anti-VEGF antibody or 2C3-based therapeutic. Generally,the two agents are administered at times effectively spaced apart toallow the two agents to exert their respective therapeutic effects,i.e., they are administered at “biologically effective time intervals”.The at least a second anti-cancer agent may be administered to theanimal or patient at a biologically effective time prior to theVEGFR2-blocking, anti-VEGF antibody or 2C3-based therapeutic, or at abiologically effective time subsequent to that therapeutic.

Accordingly, the present invention provides methods for treating ananimal or patient with a vascularized tumor, comprising:

(a) subjecting the animal or patient to a first treatment thatsubstantially reduces the tumor burden; and

(b) subsequently administering at least a first anti-angiogenic agent tothe animal or patient in an amount effective to inhibit metastasis fromany surviving tumor cells; wherein the first anti-angiogenic agent is atleast a first VEGFR2-blocking, anti-VEGF antibody, or antigen-bindingfragment thereof, optionally one that binds to substantially the sameepitope as the monoclonal antibody 2C3 (ATCC PTA 1595); optionallywherein the antibody or fragment is operatively associated with a secondanti-angiogenic agent.

Preferred first treatments include surgical resection andchemotherapeutic intervention. Combined anti-angiogenics can also beused, such as angiopoietin 2 or tumor-targeted angiopoietin 2constructs.

Other treatment methods for animals or patients with vascularizedtumors, comprise:

(a) administering a first antibody-therapeutic agent construct to theanimal or patient in an amount effective to induce substantial tumornecrosis; wherein the first antibody-therapeutic agent constructcomprises a therapeutic agent operatively linked to a first antibody, orantigen binding fragment thereof, that binds to a surface-expressed,surface-accessible or surface-localized component of a tumor cell, tumorvasculature or tumor stroma; and

(b) subsequently administering a second antibody to the animal orpatient in an amount effective to inhibit metastasis from any survivingtumor cells; wherein the second antibody is at least a firstVEGFR2-blocking, anti-VEGF antibody, or antigen-binding fragmentthereof, optionally one that binds to substantially the same epitope asthe monoclonal antibody 2C3 (ATCC PTA 1595); and further optionallywherein the antibody or fragment is operatively associated with a secondanti-angiogenic agent.

In particularly preferred embodiments, the present invention providesVEGFR2-blocking, anti-VEGF antibodies and 2C3-based antibodies for usein combination with prodrugs and ADEPT. In such compositions,combination, pharmaceuticals, kits, methods and uses, theVEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody or fragmentthereof will be modified to provide a converting or enzymatic capacity,or operatively associated with, preferably covalently linked orconjugated to, at least a first converting agent or enzyme capable ofconverting at least one prodrug to the active form of the drug.

The enzymatic or enzyme-conjugated antibody or fragment will combinedwith an initially separate formulation of the “prodrug”. The prodrugwill be an inactive or weakly active form of a drug that is that isconverted to the active form of the drug on contact with the enzymaticcapacity, converting function or enzyme associated with theVEGFR2-blocking, anti-VEGF or 2C3 antibody.

Accordingly, kits are provided that comprise, preferably in separatecompositions and/or containers:

(a) a biologically effective amount of at least a first VEGFR2-blocking,anti-VEGF antibody or 2C3-based antibody, or fragment thereof, that hasan enzymatic function, preferably where the antibody or fragment isoperatively associated with, covalently linked or conjugated to, atleast a first enzyme; and

(b) a biologically effective amount of at least a first substantiallyinactive prodrug that is converted to a substantially active drug by theenzymatic function of, or enzyme associated with, linked to orconjugated to the VEGFR2-blocking, anti-VEGF or 2C3 antibody orfragment.

The present invention further provides advantageous methods and usesthat comprise:

(a) administering to an animal or patient with a vascularized tumor abiologically effective amount of at least a first pharmaceuticalcomposition comprising at least a first VEGFR2-blocking, anti-VEGFantibody or 2C3-based antibody, or antigen binding fragment thereof,wherein the antibody or fragment has an enzymatic function, preferablywherein the antibody or fragment is operatively associated with,covalently linked to, or conjugated to, at least a first enzyme; whereinsaid antibody or fragment localizes to the vasculature, intratumoralvasculature or stroma of the vascularized tumor after adminstration; and

(b) subsequently administering to the animal or patient, after aneffective time period, a biologically effective amount of at least asecond pharmaceutical composition comprising a biologically effectiveamount of at least one substantially inactive prodrug; wherein theprodrug is converted to a substantially active drug by the enzymaticfunction of, or enzyme associated with, linked to, or conjugated to theVEGFR2-blocking, anti-VEGF or 2C3 antibody or fragment localized withinthe vasculature, intratumoral vasculature or stroma of said vascularizedtumor.

In certain other embodiments, the antibodies and immunoconjugates of theinvention may be combined with one or more diagnostic agents, typicallydiagnostic agents for use in connection with angiogenic diseases. Arange of diagnostic compositions, kits and methods are thus includedwithin the invention.

In terms of cancer diagnosis and treatment, the diagnostic and imagingcompositions, kits and methods of the present invention include in vivoand in vitro diagnostics. For example, a vascularized tumor may beimaged using a diagnostically effective amount of a tumor diagnosticcomponent that comprises at least a first binding region that binds toan accessible component of a tumor cell, tumor vasculature or tumorstroma, operatively attached to an in vivo diagnostic imaging agent.

The tumor imaging is preferably conducted to provide an image of thestroma and/or vasculature of a vascularized tumor using a diagnosticcomponent that comprises at least a first binding region that binds toan accessible component of tumor vasculature or tumor stroma. Anysuitable binding region or antibody may be employed, such as thosedescribed above in terms of the therapeutic constructs. Certainadvantages will be provided by using a detectably-labeledVEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody construct,wherein the image formed will be predictive the binding sites of thetherapeutic to be used.

Detectably-labeled in vivo tumor diagnostics, whether VEGFR2-blocking,anti-VEGF antibody or 2C3-based or not, may comprise an X-ray detectablecompound, such as bismuth (III), gold (III), lanthanum (III) or lead(II); a radioactive ion, such as copper⁶⁷, gallium⁶⁷, gallium⁶⁸,indium¹¹¹′, indium¹²³, iodine¹²³, iodine¹²⁵, iodine¹³¹, mercury¹⁹⁷,mercury²⁰³, rhenium¹⁸⁶, rhenium¹⁸⁸, rubidium⁹⁷, rubidium¹⁰³,technetium^(99m) or yttrium⁹⁰; a nuclear magnetic spin-resonanceisotope, such as cobalt (II), copper (II), chromium (III), dysprosium(III), erbium (III), gadolinium (III), holmium (III), iron (II), iron(III), manganese (II), neodymium (III), nickel (II), samarium (III),terbium (III), vanadium (II) or ytterbium (III); or rhodamine orfluorescein.

Pre-imaging before tumor treatment may be carried out by:

(a) administering to the animal or patient a diagnostically effectiveamount of a pharmaceutical composition comprising a diagnostic agentoperatively attached to at least a first binding region that binds to anaccessible component of a tumor cell, tumor vasculature (preferably) ortumor stroma (preferably), including diagnostic agents operativelyattached to VEGFR2-blocking, anti-VEGF antibody or 2C3-based antibodyconstructs; and

(b) subsequently detecting the detectably-labeled first binding region(or VEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody) bound tothe tumor cells, tumor blood vessels (preferably) or tumor stroma(preferably); thereby obtaining an image of the tumor, tumor vasculatureand/or tumor stroma.

Cancer treatment may also be carried out by:

(a) forming an image of a vascularized tumor by administering to ananimal or patient having a vascularized tumor a diagnostically minimalamount of at least a first detectably-labeled tumor binding agent,preferably a VEGFR2-blocking, anti-VEGF antibody or 2C3-based antibodyconstruct, comprising a diagnostic agent operatively attached to thetumor binding agent or VEGFR2-blocking, anti-VEGF antibody or 2C3-basedantibody, thereby forming a detectable image of the tumor, tumorvasculature (preferably), or tumor stroma (preferably); and

(b) subsequently administering to the same animal or patient atherapeutically optimized amount of at least a first nakedVEGFR2-blocking, anti-VEGF antibody or 2C3 antibody or therapeuticagent-antibody construct using such an antibody, thereby causing ananti-tumor effect.

Imaging and treatment formulations or medicaments are thus provided,which generally comprise:

(a) a first pharmaceutical composition comprising a diagnosticallyeffective amount of a detectably-labeled tumor binding agent, preferablya VEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody construct,that comprises a detectable agent operatively attached to the tumorbinding agent or VEGFR2-blocking, anti-VEGF antibody or 2C3-basedantibody; and

(b) a second pharmaceutical composition comprising a therapeuticallyeffective amount of at least one naked VEGFR2-blocking, anti-VEGFantibody or 2C3 antibody or therapeutic agent-antibody construct usingsuch an antibody.

The invention also provides in vitro diagnostic kits comprising at leasta first composition or pharmaceutical composition comprising abiologically effective amount of at least one diagnostic agent that isoperatively associated with at least a first VEGFR2-blocking, anti-VEGFantibody, optionally one that binds to substantially the same epitope asthe monoclonal antibody 2C3 (ATCC PTA 1595), or an antigen-bindingfragment thereof.

The invention still further provides combined kits in which thediagnostic agent is intended for use outside the body, preferably inconnection with a test conducted on a biological sample obtained from ananimal or patient. As such, the invention provides kits comprising,generally in at least two distinct containers, at least a firstcomposition, pharmaceutical composition or medicinal cocktail comprisinga biologically effective amount of at least a first VEGFR2-blocking,anti-VEGF antibody, optionally one that binds to substantially the sameepitope as the monoclonal antibody 2C3 (ATCC PTA 1595), or anantigen-binding fragment or immunoconjugate of such an anti-VEGFantibody; and a biologically effective amount of at least one diagnosticagent, component or system for in vitro use.

The “diagnostic agent, component or system for in vitro use” will be anydiagnostic agent or combination of agents that allow the diagnosis ofone or more diseases that have an angiogenic component. The in vitrodiagnostics thus include those suitable for use in generating diagnosticor prognostic information in relation to a disease or disorder asdisclosed in any one of U.S. Pat. Nos. 5,712,291, 5,753,230, 5,972,922,5,639,757, WO 98/45331 and WO 98/16551, each specifically incorporatedherein by reference.

In terms of cancer diagnosis and treatment, the in vitro diagnosticswill preferably include a diagnostic component that comprises at least afirst binding region that binds to an accessible component of a tumorcell, tumor vasculature (preferably) or tumor stroma (preferably)operatively attached to a “detectable or reporter agent” directly orindirectly detectable by an in vitro diagnostic test. “Detectable orreporter agents” directly detectable in vitro include those such asradiolabels and reporter agents detectable by immunofluorescence.

“Detectable or reporter agents” indirectly detectable in vitro includethose that function in conjunction with further exogenous agent(s), suchas detectable enzymes that yield a colored product on contact with achromogenic substrate. Indirect detection in vitro also extends todetectable or reporter components or systems that comprise the firstbinding region that binds to an accessible component of a tumor cell,tumor vasculature (preferably) or tumor stroma (preferably) incombination with at least one detecting antibody that hasimmunospecificity for the first binding region. The “detecting antibody”is preferably a “secondary antibody” that is attached to a direct orindirect detectable agent, such a radiolabel or enzyme. Alternatively, a“secondary and tertiary antibody detection system” may be used,including a first detecting antibody that has immunospecificity for thefirst binding region in combination with a second detecting antibodythat has immunospecificity for the first detecting antibody, the seconddetecting antibody being attached to a direct or indirect detectableagent.

BRIEF DESCRIPTION OF THE DRAWINGS

The following drawings form part of the present specification and areincluded to further demonstrate certain aspects of the presentinvention. The invention may be better understood by reference to one ormore of these drawings in combination with the detailed description ofspecific embodiments presented herein.

FIG. 1. 2C3 Inhibits VEGF-mediated growth of ABAE cells. ABAE cells weregrown in the presence of the various indicated antibodies and 0.5 nMVEGF. Growth after 4 days was determined colorimetrically by theenzymatic conversion of MTS (Owen's reagent) to a yellow formazan.Results are displayed as a percentage of formazan production in controlwells that were grown with VEGF alone. Background was determined bygrowing cells without VEGF or antibody and was subtracted from thecontrol and sample wells. Results show the arithmetic mean of triplicatedeterminations, the standard deviations of which were always less than20% of the mean. Shown are the growth curves for the anti-VEGF IgGantibodies including mAb 4.6.1 as a positive control and an IgG ofirrelevant specificity (Control IgG) as a negative control.

FIG. 2. 2C3 blocks VEGF binding to VEGFR2 but not VEGFR1 in ELISA. Wellswere coated with the extracellular domain of VEGFR1 (Flt-1/Fc) or VEGFR2(sFlk-1) and were then incubated with VEGF alone at 1 nM or VEGF in thepresence of the indicated IgG at either 100 nM or 1000 nM. The plate wasthen incubated with rabbit anti-VEGF (A-20, Santa Cruz Biotechnology,Inc.) at 1 μ/ml and developed using a peroxidase conjugated goatanti-rabbit antibody. Assays were performed in triplicate. Mean percentbinding in the absence of antibody is shown, together with the standarddeviation. Asterisks indicate values that are statisticallysignificantly different (p<0.002) from those in the absence of antibodyby Student's paired T-test.

FIG. 3A and FIG. 3B. 2C3 inhibits the in vivo growth of human tumorxenografts. FIG. 3A: 1×10⁷ NCI-H358 NSCLC cells were injectedsubcutaneously into nu/nu mice on day 0. FIG. 3B: 5×10⁶ A673rhabdomyosarcoma cells were injected subcutaneously into nu/nu mice onday 0. Mice were injected i.p. with the indicated IgG on day 1 and 2times/week thereafter. 2C3 was given at a dose of 100, 10, or 1μg/injection while a control IgG of irrelevant specificity (FIG. 3A) and3E7 (FIG. 3B) were also given at 100 μg/injection. Tumors were measured2-3 times per week. Mean and standard error is shown for the duration ofthe study in FIG. 3A, while data for the last day of the study (day 26)is shown in FIG. 3B.

FIG. 4. 2C3 treatment reduces the size of established human NCI-H358NSCLC tumor xenografts. Mice bearing subcutaneous NCI-H358 tumors,approximately 300-450 mm³ in size, were treated i.p. with 50 μg or 100μg of 2C3 (n=14), mAb 4.6.1 (n=5), 3E7 (n=12) or a control IgG (n=9) atthe indicated time points. Mean tumor volume along with the SEM over 116days is shown.

FIG. 5A and FIG. 5B. Comparison of 2C3 and 3E7 treatment of establishedhuman tumor xenografts. FIG. SA: Mice bearing subcutaneous NCI-H358tumors, approximately 450 mm³ in size, were treated with either 2C3(n=6) or 3E7 (n=4). Treatments (T) were 100 μg of the IgG given i.p.,except for the initial treatment that consisted of 500 μg of the IgGgiven i.v. Mean tumor volume along with the SEM is shown. At the end ofthe study (day 116), the mice were sacrificed and the tumors dissectedout and weighed. The mean tumor weight for the 2C3 treated group was0.054 g, while the 3E7 treated group had a mean tumor weight of 0.545 g.FIG. 5B: Mice bearing subcutaneous HT1080 tumors approximately 200-250mm3 in size were treated i.p. with 100 μg of 2C3 (n=9), 3E7 (n=11),control saline (n=11). The mice were treated every other day asindicated (T). The non-2C3 treated mice were sacrificed on day 26 due tomore than 50% of each group having large ulcerated tumors. Mean tumorvolume along with the SE is shown.

DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

Solid tumors and carcinomas account for more than 90% of all cancers inman. Although the use of monoclonal antibodies and immunotoxins has beeninvestigated in the therapy of lymphomas and leukemias, these agentshave been disappointingly ineffective in clinical trials againstcarcinomas and other solid tumors (Abrams and Oldham, 1985). A principalreason for the ineffectiveness of antibody-based treatments is thatmacromolecules are not readily transported into solid tumors. Even oncewithin a tumor mass, these molecules fail to distribute evenly due tothe presence of tight junctions between tumor cells, fibrous stroma,interstitial pressure gradients and binding site barriers (Dvorak etal., 1991 a).

In developing new strategies for treating solid tumors, the methods thatinvolve targeting the vasculature of the tumor, rather than the tumorcells, offer distinct advantages. An effective destruction or blockadeof the tumor vessels arrests blood flow through the tumor and results inan avalanche of tumor cell death. Antibody-toxin and antibody-coagulantconstructs have already been effectively used in the specific targetingand destruction of tumor vessels, resulting in tumor necrosis (Burrowset al., 1992; Burrows and Thorpe, 1993; WO 93/17715; WO 96/01653; U.S.Pat. Nos. 5,855,866; 5,877,289; 5,965,132; 6,051,230; 6,004,555; U.S.Ser. No. 08/482,369, Issue Fee paid Oct. 20, 1998; each incorporatedherein by reference).

Where antibodies, growth factors or other binding ligands are used tospecifically deliver a coagulant to the tumor vasculature, such agentsare termed “coaguligands”. A currently preferred coagulant for use incoaguligands is truncated Tissue Factor (tTF) (Huang et al., 1997; WO96/01653; U.S. Pat. No. 5,877,289). TF is the major initiator of bloodcoagulation. At sites of injury, Factor VII/VIIa in the blood comes intocontact with, and binds to, TF on cells in the perivascular tissues. TheTF:VIIa complex, in the presence of the phospholipid surface, activatesfactors IX and X. This, in turn, leads to the formation of thrombin andfibrin and, ultimately, a blood clot.

A range of suitable target molecules that are available on tumorendothelium, but largely absent from normal endothelium, have beendescribed. For example, expressed targets may be utilized, such asendoglin, E-selectin, P-selectin, VCAM-1, ICAM-1, PSMA, a TIE, a ligandreactive with LAM-1, a VEGF/VPF receptor, an FGF receptor, α_(v)β₃integrin, pleiotropin or endosialin (U.S. Pat. Nos. 5,855,866; 5,877,289and 6,004,555; Burrows et al., 1992; Burrows and Thorpe, 1993; Huang etal., 1997; each incorporated herein by reference).

Other targets inducible by the natural tumor environment or followingintervention by man are also targetable entities, as described in U.S.Pat. Nos. 5,776,427 and 6,036,955; each incorporated herein byreference). When used in conjunction with prior suppression in normaltissues and tumor vascular induction, MHC Class II antigens may also beemployed as targets (U.S. Pat. Nos. 5,776,427; 6,004,554 and 6,036,955;each incorporated herein by reference).

Adsorbed targets are another suitable group, such as VEGF, FGF, TGFβ,HGF, PF4, PDGF, TIMP, a ligand that binds to a TIE or a tumor-associatedfibronectin isoform (U.S. Pat. Nos. 5,877,289 and 5,965,132; eachincorporated herein by reference). Fibronectin isoforms are ligands thatbind to the integrin family of receptors. Tumor-associated fibronectinisoforms are targetable components of both tumor vasculature and tumorstroma.

One currently preferred marker for such clinical targeting applicationsis receptor-associated VEGF. In fact, assemblies of VEGF:receptorcomplexes are one of the most specific markers of tumor vasculatureobserved to date (U.S. Pat. Nos. 5,877,289; 5,965,132 and 6,051,230;Lin-Ke et al., 1996; Dvorak et al., 1991b).

The VEGF:receptor complex presents an attractive target for the specificdelivery of drugs or other effectors to tumor endothelium—as tumors arerich in cytokines and growth factors and as VEGF receptors areupregulated under the hypoxic conditions that are found in most solidtumors (Mazure et al., 1996; Forsythe et al., 1996; Waltenberger et al.,1996; Gerber et al, 1997; Kremer et al., 1997). Upregulation of both theligand and its receptor specifically in the tumor microenvironment leadsto a high concentration of occupied receptor on tumor vascularendothelium, as compared with the endothelium in normal tissue (U.S.Pat. Nos. 5,877,289 and 5,965,132). Dvorak and colleagues also showedthat rabbit polyclonal antibodies directed against the N-terminus ofVEGF selectively stain tumor blood vessels after injection into micebearing syngeneic tumors (Lin-Ke et al., 1996).

The role of VEGF as a target for clinical intervention is not limited toimmunotoxin or coaguligand therapies. Indeed, VEGF is one of the keyfactors involved in angiogenesis of solid tumors (Ferrara, 1995; Potgenset al., 1995), being both a potent permeability agent (Senger et al.,1983; Senger et al., 1990; Senger et al., 1986) and endothelial cellmitogen (Keck et al., 1989; Connolly et al., 1989; Thomas, 1996). Thelink between VEGF and angiogenesis has led to proposals of varioustherapeutic strategies aimed at VEGF intervention (Siemeister et al.,1998).

A. VEGF and VEGF Receptors

Vascular endothelial growth factor (VEGF) is a multifunctional cytokinethat is induced by hypoxia and oncogenic mutations. VEGF is a primarystimulant of the development and maintenance of a vascular network inembryogenesis. It functions as a potent permeability-inducing agent, anendothelial cell chemotactic agent, an endothelial survival factor, andendothelial cell proliferation factor (Thomas, 1996; Neufeld et al.,1999). Its activity is required for normal embryonic development (Fonget al., 1995; Shalaby et al., 1995), as targeted disruption of one orboth alleles of VEGF results in embryonic lethality (Carmeliet et al.,1996; Ferrara et al., 1996)

VEGF is an important factor driving angiogenesis or vasculogenesis innumerous physiological and pathological processes, including woundhealing (Frank et al., 1995; Burke et al., 1995), diabetic retinopathy(Alon et al., 1995; Malecaze et al., 1994), psoriasis (Detmar et al.,1994), atherosclerosis (Inoue et al., 1998), rheumatoid arthritis(Harada et al., 1998; Nagashima et al., 1999), solid tumor growth (Plateet al., 1994; Claffey et al., 1996).

A wide variety of cells and tissues produce VEGF, which exists in atleast five isoforms (121, 145, 165, 189, and 206 amino acids) that aresplice variants encoded by the same gene (Houck et al., 1991; Ferrara etal., 1991; Tischer et al., 1991). The two smaller isoforms, 121 and 165,are secreted from cells (Houck et al., 1991; Anthony et al., 1994).Secreted VEGF is an obligate dimer of between 38-46 kDa in which themonomers are linked by two disulfide bonds.

VEGF dimers bind with high affinity to two well-characterized receptors,VEGFR1 (FLT-1) and VEGFR2 (KDR/Flk-1), which are selectively expressedon endothelial cells (Flt-1 and Flk-1 are the mouse homologues). TheK_(d) of VEGF binding to VEGFR1 and VEGFR2 is 15-100 pM and 400-800 pM,respectively (Terman et al, 1994). A recently identified third cellsurface protein, neuropilin-1, also binds VEGF with high affinity(Olander et al, 1991; De Vries et al, 1992; Terman et al., 1992; Sokeret al, 1998).

VEGFR1 and VEGFR2 are members of the Type III receptor tyrosine kinase(RTK III) family that is characterized by seven extracellular IgG-likerepeats, a single spanning transmembrane domain, and an intracellularsplit tyrosine kinase domain (Mustonen and Alitalo, 1995). Until veryrecently, VEGFR1 and VEGFR2 were thought to be almost exclusivelyexpressed on endothelial cells (Mustonen and Alitalo, 1995). AlthoughVEGFR1 and VEGFR2 have been reported to have different functions withrespect to stimulating endothelial cell proliferation, migration, anddifferentiation (Waltenberger et al., 1994; Guo et al., 1995), theprecise role that each receptor plays in VEGF biology and endothelialcell homeostasis was not clearly defined prior to the present invention.

Recent studies using knockout mice have shown each of VEGF, VEGFR1 andVEGFR2 to be essential for vasculogenesis, angiogenesis and embryodevelopment (Fong et al., 1995; Shalaby et al., 1995; Hiratsuka et al.,1998). In studies of lethal knockouts, the phenotypes associated withthe lack of each receptor were different. Targeted disruption of VEGFR2resulted in an embryo that lacked endothelial cell differentiation andfailed to form yolk sac blood islands or go through vasculogenesis(Shalaby et al., 1995). VEGFR1 null mutants showed impairedvasculogenesis, disorganized assembly of endothelial cells, and dilatedblood vessels (Fong et al., 1995; Hiratsuka et al., 1998). VEGFR1evidently has a vital biological role.

VEGFR1 has a higher affinity for VEGF than VEGFR2, although it has alower tyrosine kinase activity. This suggests that the extracellulardomain of VEGFR1 is particularly important. This hypothesis was stronglysupported by results from studies in knockout mice in which the tyrosinekinase domain of VEGFR1 was deleted whilst leaving the VEGF bindingdomain intact (Hiratsuka et al., 1998). The VEGFR1-tyrosine kinasedeficient embryos developed normal blood vessels and survived to term(Hiratsuka et al., 1998).

In addition to the earlier knockouts (Fong et al., 1995; Shalaby et al.,1995), the Hiratsuka et al. (1998) studies indicate that VEGFR 1 has avital biological role. However, tyrosine kinase signaling does not seemto be the critical factor. It is interesting to note that macrophagesfrom the VEGFR1 knockout mice did not exhibit VEGF-induced chemotaxis(Hiratsuka et al., 1998; incorporated herein by reference), therebyimplicating VEGFR I as the receptor responsible for mediating thisimportant biological response to VEGF.

Certain groups have reported VEGFR2 to be the dominant signalingreceptor in VEGF-induced mitogenesis, and permeability (Waltenberger etal., 1994; Zachary, 1998; Korpelainen and Alitalo, 1998). The role ofVEGFR1 in endothelial cell function is much less clear, althoughfunctions in macrophage migration and chemotaxis were documented in theHiratsuka et al. (1998) studies discussed above.

Clauss et al. (1996; incorporated herein by reference) also reportedthat VEGFR1 has important roles in monocyte activation and chemotaxis.In fact, cells of the macrophage/monocyte lineage express only VEGFR1,which is the receptor responsible for mediating monocyte recruitment andprocoagulant activity (Clauss et al., 1996). VEGF binding to VEGFR1 onmonocytes and macrophages also acts by raising intracellular calcium andinducing tyrosine phosphorylation (Clauss et al., 1996).

Binding of the VEGF dimer to the VEGF receptor is believed to inducereceptor dimerization. Dimerization of the receptor then causesautotransphosphorylation of specific tyrosine residues, Y801 and Y1175,and Y1213 and Y1333 on the intracellular side of VEGFR2 and VEGFR1,respectively. This leads to a signal transduction cascade. whichincludes activation of phospholipase Cγ(PLCγ) and phosphatidylinositol3-kinase (PI3K) and an increase in intracellular calcium ions (Hood andMeininger, 1998; Hood et al., 1998; Kroll and Waltenberger, 1998).

The intracellular events further downstream in VEGF-induced signalingare less clear, although a number of groups have shown that nitric oxide(NO) is produced after VEGF activation of VEGFR2 (Hood and Meininger,1998; Hood et al., 1998; Kroll and Waltenberger, 1998). Activation ofVEGFR2, but not VEGFR1, by VEGF has also been shown to activate Src andthe Ras-MAP kinase cascade, including the MAP kinases, ERK 1 and 2(Waltenberger et al., 1994, 1996; Kroll and Waltenberger, 1997).

The role of VEGFR1 in endothelial cell function is much less clear,particularly as Flt-1 tyrosine kinase-deficient mice are viable anddevelop normal vessels (Hiratsuka et al., 1998). It has been suggestedthat the main biological role of VEGFR1 on endothelial is as anon-signaling ligand-binding molecule, or “decoy” receptor that might berequired to present VEGF to VEGFR2.

The connection between VEGF and pathological angiogenic conditions hasprompted various attempts to block VEGF activity. These include thedevelopment of certain neutralizing antibodies against VEGF (Kim et al.,1992; Presta et al., 1997; Sioussat et al., 1993; Kondo et al., 1993;Asano et al., 1995). Antibodies against VEGF receptors have also beendescribed, such as described in U.S. Pat. Nos. 5,840,301 and 5,874,542and, subsequent to the present invention, in WO 99/40118. U.S. Pat. Nos.5,840,301 and 5,874,542 indeed suggest that blocking VEGF receptorsrather than VEGF itself is advantageous for various reasons.

Soluble receptor constructs (Kendall and Thomas, 1993; Aiello et al.,1995; Lin et al., 1998; Millauer et al, 1996), tyrosine kinaseinhibitors (Siemeister et al., 1998), antisense strategies, RNA aptamersand ribozymes against VEGF or VEGF receptors have also been reported(Saleh et al., 1996; Cheng et al., 1996; Ke et al., 1998; Parry et al.,1999; each incorporated herein by reference).

B. Anti-VEGF Antibodies

B1. Range of Antibody Properties

The application of various inhibitory methods has been shown to be atleast somewhat effective in either blocking angiogenesis and/orsuppressing tumor growth by interfering with VEGF signaling. In fact,monoclonal antibodies against VEGF have been shown to inhibit humantumor xenograft growth and ascites formation in mice (Kim et al., 1993;Asano et al., 1995; 1998; Mesiano et al., 1998; Luo et al., 1998a;1998b; Borgstrom et al., 1996; 1998).

The antibody A4.6.1 is a high affinity anti-VEGF antibody capable ofblocking VEGF binding to both VEGFR1 and VEGFR2 (Kim et al., 1992;Wiesmann et al., 1997; Muller et al,1998). Alanine scanning mutagenesisand X-ray crystallography of VEGF bound by the Fab fragment of A4.6.1showed that the epitope on VEGF that A4.6.1 binds is centered aroundamino acids 89-94. This structural data demonstrates that A4.6.1competitively inhibits VEGF from binding to VEGFR2, but inhibits VEGFfrom binding to VEGFR1 most likely by steric hindrance (Muller et al ,1998; Keyt et al., 1996; each incorporated herein by reference)

A4.6.1 is the most extensively utilized neutralizing anti-VEGF antibodyin the literature to date. It has been shown to inhibit the growth andVEGF-induced vascular permeability of a variety of human tumors in mice(Brem, 1998; Baca et al., 1997; Presta et al., 1997; Mordenti et al.,1999; Borgstrom et al., 1999; Ryan et al., 1999; Lin et al., 1999; eachspecifically incorporated herein by reference). A4.6.1 also inhibitsascites formation in a well-characterized human ovarian carcinoma mousemodel and tumor dissemination in a novel metastasis mouse model. A4.6.1has recently been humanized by monovalent phage display techniques andis currently in Phase I clinical trials as an anti-cancer agent (Brem,1998; Baca et al., 1997; Presta et al., 1997; each incorporated hereinby reference).

Despite some success in the art with neutralizing antibodies againstVEGF, the present inventors realized that new antibodies, particularlythose with a more precisely defined mode of interaction with VEGFR1(FLT-1) and/or VEGFR2 (KDR/Flk-1) would of benefit for a variety ofreasons. For example, the development of anti-VEGF antibodies thatselectively block the interaction of VEGF with only one of the two VEGFreceptors would allow for a more precise dissection of the pathwaysactivated by VEGF in cells that express both VEGFR1 and VEGFR2.

The present inventors believed that antibodies of definedepitope-specificity that blocked VEGF binding to only one receptor(VEGFR2s) may well have clinical benefits depending, of course, on themaintenance of their inhibitory effects in an in vivo environment. Theknockout mice studies of Hiratsuka et al. (1998) show that both VEGFR1and VEGFR2 have important biological roles. Prior to the presentinvention, realistic opportunities for therapeutic intervention aimed atinhibiting VEGF-mediated effects through only one of the two receptorswere hampered by the lack of effective, tailored inhibitory agents.

The present inventors first developed a range of new anti-VEGFantibodies having various epitope-specificities and properties. Sixgroups of hybridomas that secrete monoclonal antibodies against theVEGF:receptor (Flk-1) complex or against VEGF itself are provided. Fiveof antibody groups do not interfere with the binding of VEGF to itsreceptor, while one blocked this interaction (2C3 group) and inhibitedVEGF-mediated growth of endothelial cells.

Antibodies of the 3E7, GV39M, and 2C3 groups, all of which localizeselectively to the tumor after intravenous injection into mice bearinghuman tumor xenografts, are currently preferred for use in targeting,imaging and treating the vasculature or connective tissue of solidtumors.

The monoclonal antibodies of the present invention that recognize theVEGF:receptor complex selectively localize to tumor endothelial cellsafter injection into mice bearing human tumor xenografts. The monoclonalantibodies of the 2C3 group localize conspicuously to the perivascularconnective tissue of the tumor, and also to the surrounding tumorvessels.

The antibodies that recognize the N-terminus react with receptor boundVEGF by ELISA. GV39M and 11B5 display high specificity forreceptor-bound VEGF, as opposed to non-receptor-bound VEGF. Presumablythe epitope recognized by GV39M and 11B5 on the N-terminus isconformational and is created when VEGF binds to its receptor. The factthat the antibodies are both IgMs, and therefore large in size, may beimportant for their selectivity toward the VEGF:receptor complex.

The anti-N-terminal antibodies did not inhibit VEGF-mediated endothelialcell growth. This suggests that the N-terminus of VEGF is not involvedin receptor interaction and that antibodies against the N-terminus ofVEGF do not interfere with VEGF-mediated signaling.

In contrast, 2C3 inhibits VEGF-mediated growth of endothelial cells withan lC₅₀ of 3 nM. ¹²⁵I-VEGF binding studies using KDR expressingendothelial cells (ABAE cells) demonstrated that 2C3 blocks VEGF frombinding to KDR in a concentration dependent manner. Thus, 2C3 is capableof neutralizing KDR (VEGFR2) mediated VEGF activity in vitro byinterfering with the binding of VEGF to its receptor.

Immunohistochemical analyses revealed that GV39M, 11B5, 3E7, and 7G3react moderately to strongly with vascular endothelium when directlyapplied to the sections. GV39M displays the highest specificity fortumor endothelial cells with comparatively little staining of tumorcells or connective tissue. 11B5, 3E7, and 7G3 preferentially stainendothelial cells when applied at low concentrations, but stain tumorcells and connective tissue distinctly at higher concentrations.

The pattern of staining observed with 11B5, 3E7 and 7G3 is typical ofthe type of staining seen when using polyclonal antibodies against VEGFthat do not have a preference for a particular conformation of VEGF(Lin-Ke et al., 1996; Plate et al., 1994; Claffey et al., 1996). Theselective staining of endothelium by GV39M suggests that it binds to theVEGF:receptor complex on these cells and is consistent with theendothelial cell location of the receptors and the fact that GV39M bindsselectively to VEGF:sFlk-1 in ELISA.

Similarly, the broader staining patterns of 3E7 and 7G3 are consistentwith their ability to recognize both free and receptor bound VEGF.However, 11B5 was expected to have a staining pattern that was morerestricted to endothelium because it strongly prefers VEGF:Flk-1 in thecapture ELISA (see Table 2). It is possible that 11B5 is able torecognize VEGF that is bound to stromal components, giving it a broaderreactivity pattern on tumor sections.

3E7 and GV39M selectively localize in vivo to vascular endothelial cellsof tumor tissue, while 2C3 localizes to perivascular connective tissueof tumors, in addition to the endothelium. Twenty four hours after i.v.injection into tumor-bearing mice, 3E7 was not detectable on theendothelium of any tissue except the tumor. GV39M, on the other hand,also bound to endothelial cells or mesangial cells in the glomeruli ofthe kidney. The reason for reactivity of GV39M with the mouse kidneyglomerulus is unclear. It could be that the antibody binds to theVEGF:receptor complex on the normal endothelial cells in the kidney(Takahashi et al., 1995). However, localization studies in guinea pigsbearing syngeneic Line 10 tumors have shown that GV39M localizes totumor blood vessels but not to glomeruli or vessels in other normaltissues.

The ability of 3E7 and GV39M to localize specifically to tumorendothelium is probably a result of at least two factors. First, theVEGF:receptor complex is relatively abundant on tumor blood vesselsbecause the hypoxic tumor microenvironment stimulates VEGF expression bytumor cells and VEGF receptor expression by endothelial cells. Second,tumor blood vessels are more permeable than normal blood vessels (Yuanet al., 1996), which may allow the antibody greater access to theVEGF:receptor complex that appears to be concentrated on the abluminalface of the vessels (Lin-Ke et al., 1996; Hong et al, 1995).

In a prior study by Lin-Ke and colleagues (1996), rabbit polyclonalantibodies directed against the N-terminus of rat VEGF were found tolocalize to tumor endothelial cells after injection into mice bearingTA3/St mouse mammary carcinoma or MOT ovarian carcinoma. In contrast, arabbit polyclonal antibody (Ab-618) directed against the whole VEGFprotein did not localize specifically to endothelial cells in thesetumors or elsewhere in the tumors themselves.

Based on these results, Lin-Ke et al. (1996) concluded that theN-terminus of VEGF has the capacity to bind antibodies after VEGF hasassociated with microvascular endothelium and that the pool of free ornon-endothelial cell associated VEGF is not sufficient to concentrateanti-VEGF antibodies directed against non-N-terminal epitopes (Lin-Ke etal., 1996). The present results with 3E7 and GV39M, directed against theN-terminus of VEGF support their conclusions.

However, the findings of the present invention that antibodies of the2C3 group, directed against a non-N-terminal epitope on VEGF, localizeboth to the vasculature and to the perivascular connective tissue ofsolid tumors in mice are remarkably surprising over the Lin-Ke et al.(1996) work. The present invention suggests that a ‘pool’ of VEGF ispresent in the tumor stroma and does, in fact, allow for theconcentration of 2C3 in the tumor mass. Such tumor stromal targetingcould not have been predicted from a study of prior publications. Theinventors contemplate that VEGF may bind to heparan sulfateproteoglycans (HSPGs) within the tumor, although understanding themechanism of action is certainly not necessary to practicing the presentinvention.

An early conclusion of the present invention is that antibodies of theGV39M and 3E7 groups localize selectively to tumor endothelial cells inmice, whereas antibodies of the 2C3 group localize to the tumorendothelial cells and to the perivascular connective tissue of thetumor. Since the distribution of VEGF and its receptors are similar inthe mouse and in man, these antibodies are contemplated to show similarpatterns of localization in cancer patients. Thus, GV39M and 3E7 areenvisioned for use in the delivery of therapeutic or diagnostic agentsto tumor vasculature in man, while antibodies of the 2C3 group arecontemplated as vehicles for targeting therapeutic or diagnostic agentsto tumor vasculature and tumor connective tissue.

B2. VEGFR2-blocking, Anti-VEGF and 2C3 Antibodies

Further studies on the antibodies of the 2C3 group revealed even furthersurprising properties, resulting in the effective compositions and usesof the present invention.

An important discovery of this invention, made using ELISA, receptorbinding assays and receptor activation assays, is that monoclonalantibodies of the 2C3 group selectively block the interaction of VEGFwith VEGFR2 (KDR/Flk-1), but not VEGFR1 (FLT-1). 2C3 antibodies inhibitVEGF-induced phosphorylation of VEGFR2 and block VEGF-inducedpermeability, implicating VEGFR2 as the receptor responsible forVEGF-induced permeability. 2C3 antibodies also have potent anti-tumoractivity, arresting the growth of various established human solid tumorsin art-accepted animal models of human cancer.

These discoveries demonstrate the usefulness of 2C3 in dissecting thepathways that are activated by VEGF in cells that express both VEGFR1and VEGFR2, as well as highlighting the importance of VEGFR2 activity inthe process of tumor growth and survival. More importantly, they providea unique mode of therapeutic intervention, allowing specific inhibitionof VEGFR2-induced angiogenesis, without concomitant inhibition ofmacrophage chemotaxis, osteoclast and chondroclast function (mediated byVEGFR1).

The discoveries concerning 2C3 thus provide, for the first time, themotivation and the means to make and use anti-VEGF antibodies thatinhibit VEGF binding only to VEGFR2, and not VEGFR1. Such antibodies,succinctly termed “VEGFR2-blocking, anti-VEGF antibodies”, represent anadvance in the field and provide numerous advantages, both in terms ofuses in unconjugated or “naked” form and when conjugated to orassociated with other therapeutic agents.

The in vitro binding studies of the present invention, employing ELISAand co-precipitation assays. with purified receptor proteins,demonstrated that 2C3 blocks the binding of VEGF to VEGFR2.Surprisingly, though 2C3 did not inhibit the binding of VEGF to VEGFR1in any assay system. In order to confirm the initial results, bindingELISAs were repeated in different configurations. In each configuration,the results indicated that 2C3 does not interfere with the VEGF:VEGFR1interaction. As a control for these studies the monoclonal antibody 3E7,an antibody directed against the NH₂-terminus of VEGF, was used, whichdid not block VEGF from binding to VEGFR1 or VEGFR2.

The 2C3 group of antibodies of the present invention are thussignificantly improved over other blocking antibodies to VEGF, includingA4.6.1. The A4.6.1 anti-VEGF antibody blocked the binding of VEGF toboth VEGF receptors. Crystallographic and mutagenesis studies have shownthat the binding epitopes for VEGFR2 and VEGFR1 are concentrated towardsthe two symmetrical poles of the VEGF dimer (Wiesmann et al., 1997;Muller et al., 1997). The binding determinants on VEGF that interactwith the two receptors overlap partially and are distributed over fourdifferent segments that span across the dimer surface (Muller et al.,1998). Antibody 4.6.1 binds to a region of VEGF within the receptorbinding region of both receptors (Muller et al., 1998). It is proposedthat 2C3 binds to a region that lies close to the VEGFR2 binding site,but not to the VEGFR1 binding site.

Studies on the effect of 2C3 on VEGF-induced phosphorylation of thereceptors showed that 2C3 does block VEGF-induced phosphorylation ofVEGFR2. This also corresponds to data discussed above and furthersolidifies the role of VEGFR2 in VEGF-induced proliferation.

Similar to results from other studies, consistent VEGF-inducedphosphorylation of VEGFR1 could not be demonstrated (De Vries et al.,1992; Waltenberger et al., 1994; Davis-Smyth et al, 1996; Landgren etal., 1998). Therefore, it could not be reliably judged whether 2C3inhibits VEGF-induced phosphorylation of VEGFR1. The low activity ofVEGF on VEGFR1 phosphorylation has lead others to suggest that VEGFR1might not be a signaling receptor on endothelial cells, but that itmight act as a decoy receptor to capture VEGF and amplify its signalingvia VEGFR2 (Hiratsuka et al, 1998). However, tyrosine phosphorylation ofVEGFR1 by VEGF binding has been reported by Kupprion et al. (1998) usinghuman microvascular endothelial cells (HMEC) and by Sawano et al. (1996)using NIH 3T3 cells that overexpress VEGFR1. Additionally, Waltenbergeret al. (1994) have shown that VEGF-induced VEGFR1 activation can befollowed using an in vitro kinase assay. The effect of 2C3 onVEGF-induced phosphorylation of VEGFR1, or lack thereof, could bedetermined using one of the foregoing cell types or an in vitro kinaseassay.

The present ELISA data of FIG. 2 and cell binding data demonstrate that2C3 antibodies do not completely block VEGF from binding to cells thatexpress both VEGFR1 and VEGFR2. The fact that 2C3 does not block VEGFbinding to VEGFR1 means that 2C3 antibodies will be effective tools indelineating the role of VEGFR1 in the biology of endothelial cells andother cell types.

The functional consequences of the selectivity that 2C3 shows inblocking VEGF from activating its receptors was examined using the Milespermeability assay in guinea pigs. Both 2C3 and A4.6.1 inhibitedVEGF-induced permeability when the IgG was in at least a 10-fold molarexcess over VEGF. 3E7 and control antibodies did not inhibitVEGF-induced permeability even at a 1000-fold molar excess. Theseresults show that VEGFR2 is involved in VEGF-induced permeability.

This finding accords with recent reports that a novel form of VEGF-C andtwo virus-derived VEGF-E variants bind VEGFR2 but not VEGFR1, yet retainthe ability to enhance vascular permeability (Joukov et al., 1998; Ogawaet al., 1998; Meyer et al., 1999). Probably, the various forms of VEGFtransmit signals via VEGFR2 that cause NO production, which, in turn,causes the increase in vascular permeability (Hood and Granger, 1998;Hood et al., 1998; Kroll and Waltenberger, 1998; Murohara et al., 1998;Kupprion et al., 1998; Sawano et al., 1996; Fujii et al., 1997; Parentiet al., 1998). This points indirectly at VEGFR2 involvement, as NOproduction has been shown to a consequence of VEGFR2 activation.However, there is also some evidence to the contrary, as Couper et al.(1997), found a strong correlation between increased vascularpermeability induced by VEGF and VEGFR1 expression in vivo.

2C3 inhibited the growth of multiple different human tumor types invivo. The effect of 100 μg of 2C3 given twice/wk was identical inmice-bearing subcutaneous NCI-H358 NSCLC and A673 rhabdomyosarcomatumors, where it effectively limited the growth of the tumors to a smallnodule of approximately 150 mm³ in size. Similar responses were seen inother tumor models, such as HT29 and LS174T, both human adenocarcinomasof the colon.

The magnitude of tumor growth suppression by 2C3 is similar to thatreported by other investigators using different neutralizing anti-VEGFantibodies (Asano et al., 1998; Mesiano et al., 1998). A monoclonal ratanti-mouse VEGFR2 antibody also strongly blocked the growth of malignanthuman keratinocytes in mice through an anti-angiogenic mechanism (Skobeet al., 1997). The effectiveness of 2C3, being similar to what otherinvestigators have found using different anti-VEGF antibodies, furtherdemonstrates the role of VEGF in tumor angiogenesis and tumor growth.However, 2C3 should provide a safer therapeutic, based on the specificinhibitory properties discussed herein.

To analyze the effect of inhibiting VEGF activity in a setting thatwould be closer to conditions in humans, mice that had establishedtumors were treated with 2C3. In this setting, 2C3 treatmentsignificantly slowed the growth of two aggressive human tumors. A673rhabdomyosarcoma and LS174T colon adenocarcinoma tumors. 2C3 antibodiescaused significant tumor regressions in mice-bearing NCI-H358 NSCLCtumors.

Tumors treated with 2C3 or A4.6.1 regressed to 30% and 35%,respectively, of their original size after approximately 10 weeks oftreatment. In a study where the treatment was allowed to extend past 100days, even more significant regressions were observed. The resultssuggest that VEGF is providing more than just a mitotic signal for tumorendothelium.

The fact that regressions, rather than tumor stasis, was observedsuggests that VEGF is providing more than just an angiogenic signal fortumor endothelium. Benjamin et al. (1999) recently reported that tumorscontain a large fraction of immature blood vessels that have yet toestablish contact with periendothelial cells and that these bloodvessels are dependent upon VEGF for survival. It is possible thatneutralization of VEGF causes these immature blood vessels to undergoapoptosis, thereby reducing the existing vascular network in the tumorIt is also possible that a dynamic process of vascular remodeling occursin tumors, involving both vessel formation and vessel regression, andthat neutralization of VEGF prevents vessel formation leading to a netshift towards vessel regression.

The finding that 2C3 suppressed tumor growth as completely as A4.6.1 (ifnot more so) indicates a dominant role for VEGFR2 in tumor angiogenesis.The multistep process of angiogenesis requires endothelial cellchemotaxis, metalloproteinase production, invasion, proliferation anddifferentiation. VEGFR1 may have no role in these processes, or mayassist in the processes by binding VEGF and presenting it to thesignaling receptor, VEGFR2.

The comparable figures for 2C3 and A4.6.1 in tumor treatment are highlyrelevant: 2C3 is slightly more effective as A4.6.1, although it onlybinds to VEGFR2 and not VEGFRα_(v)β₃ 1. The present studies thereforeindicate that VEGFR1 does not play a notable role in VEGF-mediated tumorangiogenesis, and further suggest that VEGFR1 specific inhibitors maynot influence tumor angiogenesis. These results also signify that 2C3can be equally or more effective than A4.6. 1, whilst causing lessside-effects.

The ability to specifically block VEGF binding to and activation ofVEGFR2 has importance in at two areas of clinical relevance. First,VEGFR1 (Flt-1) is believed to play an important role in the recruitmentof macrophages and monocytes into the tumor, as these cells expressVEGFR1 and respond chemotactically to VEGF via VEGFR1 signaling (Clausset al., 1996; Hiratsuka et al., 1998; Akuzawa et al., 2000). Uponactivation of macrophages, flt-1 gene transcription is stimulatedthrough an induction of Egr-1, which binds to overlapping Egr-1/Sp1transcription factor-binding sites in the human flt-1 promoter,providing evidence that the flt-1 gene is a direct target of Egr-1, thetranscription factor primarily induced on macrophage differentiation(Akuzawa et al., 2000).

In order to maintain activation of macrophages, as required to produce arigorous anti-tumor response, inhibition of VEGFR1 signaling should beavoided. The specific blocking of VEGFR1 afforded by the presentinvention thus provides important advantages over A4.6. 1 in tumortherapy, as macrophage infiltration will not be impaired, enabling thesecells to remove tumor cell debris from necrotic tumors and promote tumorshrinkage. Using VEGFR2-blocking, anti-VEGF antibodies, such as 2C3,will also allow the infiltrating macrophages to contribute to theoverall anti-tumor effect by having a direct cytocidal effect on tumorcells.

Indeed, the present invention provides uniquely advantageous agents foruse in all forms of anti-angiogenic therapy, due to their ability toblock VEGF angiogenic activity, but not to inhibit other beneficialactions of VEGF, mediated through VEGFR1, such as those on immune andbone cells. A second area of clinical importance concerns the ability ofantibodies prepared in accordance with this invention to function invivo without inhibiting the beneficial effects of osteoclasts andchondroclasts. This means that use of the present VEGFR2-blocking,anti-VEGF antibody therapeutics, including 2C3, will not be associatedwith side effects on bone and/or cartilage.

In vivo studies have shown that VEGF couples hypertrophic cartilageremodeling, ossification and angiogenesis during endochondral boneformation and that VEGF is essential for cartilage remodeling (Gerber etal., 1999; specifically incorporated herein by reference). Inactivationof VEGF signaling through VEGFR1, by administration of the solubleVEGFR1 receptor chimeric protein (Flt-(1-3)-IgG), was shown to impairtrabecular bone formation and the expansion of the hypertrophicchondrocyte zone by decreasing the recruitment and/or differentiation ofchondroclasts (Gerber et al., 1999).

It has further been shown that VEGF can substitute for macrophagecolony-stimulating factor (M-CSF) in the support of osteoclast functionin vivo (Niida et al., 1999; specifically incorporated herein byreference). In studies using osteopetrotic (op/op) mice with adeficiency in osteoclasts resulting from a mutation in the M-CSF gene,injection of recombinant human M-CSF (rhM-CSF) allows osteoclastrecruitment and survival. In recent studies, it was shown that a singleinjection of recombinant human VEGF can similarly induce osteoclastrecruitment in op/op mice (Niida et al., 1999).

Niida et al. (1999) reported that as osteoclasts predominantly expressVEGFR 1, and the activity of recombinant human placenta growth factor 1on osteoclast recruitment was comparable to that of rhVEGF, thebeneficial effects of VEGF signaling in osteopetrotic (op/op) mice aremediated via the VEGF receptor 1 (VEGFR-1). These authors further showedthat rhM-CSF-induced osteoclasts died after VEGF was inhibited (using aVEGFR1 receptor chimeric protein, VEGFR1/Fc), but that such effects wereabrogated by concomitant injections of rhM-CSF. Osteoclasts supported byrhM-CSF or endogenous VEGF showed no significant difference in in vivoactivity (Niida et al., 1999).

Mutant op/op mice undergo an age-related resolution of osteopetrosisaccompanied by an increase in osteoclast number. In the Niida et al.(1999) studies, most of the osteoclasts disappeared after injections ofanti-VEGF antibody, demonstrating that endogenously produced VEGF isresponsible for the appearance of osteoclasts in the mutant mice. Inaddition, rhVEGF replaced rhM-CSF in the support of in vitro osteoclastdifferentiation. These results demonstrate that M-CSF and VEGF haveoverlapping functions in the support of osteoclast function and thatVEGF acts through the VEGFR-1 receptor (Niida et al., 1999).

It can thus be concluded that 2C3, the first of the VEGFR2-blocking,anti-VEGF antibodies of the invention, does not block VEGF from bindingand activating VEGFR1, but does block VEGF from binding and activatingVEGFR2. The anti-tumor effects of such VEGFR2 inhibition are clearlydemonstrated. These results show VEGFR2 to be the VEGF receptor thatmediates permeability and highlight its role in tumor angiogenesis. Thisinvention therefore further validates VEGF inhibition as therapy for thetreatment of solid tumors. More importantly, the invention provides arange of new VEGFR2-blocking, anti-VEGF antibodies, such as those basedupon 2C3, for therapeutic intervention and, in particular, for use assafe and effective drugs for inhibiting angiogenesis in tumors and otherdiseases.

The benefits of the present invention are -not limited to the lack ofside effects. Although these are important features that will havenotable benefits, particularly in the treatment of children and patientswith bone disorders, the antibodies of the invention have numerous otheradvantages.

For example, antibody conjugates based upon the VEGFR2-blocking,anti-VEGF or 2C3 antibodies can be used to deliver therapeutic agents tothe tumor environment. In fact, 2C3 antibodies are shown herein to bindto both tumor vasculature and tumor stroma upon administration in vivo,but not to bind to vasculature or connective tissue in normal organs ortissues. Therapeutic constructs based upon the present antibodiestherefore have the advantage of combining two functions within onemolecule: the anti-angiogenic properties of the antibody or fragmentthereof and the properties of the therapeutic agent selected forattachment.

As VEGFR2 is the key receptor on endothelium, blocking VEGF binding toVEGFR2 is critical for an anti-angiogenic effect. Although VEGFR1 isexpressed on endothelium, it is non-signal transducing, or passive, inthis context. Therefore, the inability of the antibodies of the presentinvention to block VEGF binding to VEGFR1 is without consequence totheir effectiveness as anti-angiogenic and anti-tumor agents. In fact,rather than inhibiting VEGF binding to VEGFR1, which occurs with theblocking antibodies of the prior art, the ability of the presentantibodies to bind to VEGF and yet to not substantially disturbVEGF-VEGFR1 interactions enhances the drug delivery properties of thesenew antibodies.

The present inventors realized that blocking antibodies would still beexpected to function to deliver therapeutic agents to the tumorenvironment by binding to tumor-localized VEGF that is not bound to areceptor. Specifically, they understood that such antibodies will bindto VEGF in the tumor stroma and deliver therapeutic agents thereto. Thisprovides a reservoir of drug around the endothelium, causing cytotoxicor other destructive effects on the vascular endothelial cells andexerting an anti-tumor effect.

The VEGF associated with the stroma or connective tissue is not bound toa VEGF receptor in a classic sense, i.e., a cell surface receptor.Rather, VEGF is bound to one or more connective tissue components,including proteoglycans, such as heparan sulfate proteoglycan, through abasic region of VEGF. These sequences (and the exons encoding them) aremissing in VEGF121 protein (and underlying DNA), so this isoform shouldnot be present in stroma in significant amounts. VEGF in the tumorstroma is often termed “free”, although it is still localized within thetumor, so “free” essentially means non-receptor-bound.

The inventors further deduced that an antibody that blocks VEGF bindingto one, but not both receptors, would still be able to delivertherapeutic agents to the tumor environment by binding to receptor boundVEGF on the vasculature. This is one of the most advantageous featuresof the present invention. Namely, the provision of antibodies that blockVEGF binding to VEGFR2, and hence inhibit the angiogenic signal fromVEGF, but that do not block VEGF binding to VEGFR1. In addition toreducing systemic side effects by maintaining VEGF signaling via VEGFR1in other cell types and tissues, these antibodies are able to localizeto VEGF-VEGFR1 complex on tumor vasculature and to deliver therapeuticagents directly thereto.

Both VEGFR1 and VEGFR2 are upregulated on tumor endothelial cells, asopposed to endothelial cells in normal tissues. VEGFR1 is highlyexpressed on tumor vascular endothelium, which makes the targetingaspects of the present invention particularly effective. In fact,VEGFR1, although “non-signaling” in endothelium, is expressed at leastat the same levels as VEGFR2, if not at higher levels. A factorunderlying this phenomenon is that VEGFR1 is upregulated in response toboth hypoxia and VEGF, whereas VEGFR2 is only upregulated in response toVEGF and is not influenced by hypoxia.

Although the role of VEGFR1 on endothelium remains uncertain, VEGFR1 mayact as a decoy receptor to “capture” VEGF and pass the ligand onto thesignaling receptor, VEGFR2. For this to be true, one would expect thedecoy receptor to have a higher affinity for VEGF than the signalingreceptor, which is indeed the case. In light of this, and perhaps alsodue to enhanced expression levels, the VEGFR2-blocking,non-VEGFR1-blocking antibodies of this invention are ideal deliveryagents for tumor treatment. Therapeutic conjugates of these antibodiesare able to simultaneously inhibit angiogenesis through VEGFR2 anddestroy the existing vasculature by delivering a therapeutic agent toVEGF-VEGFR1 receptor complex.

The inventors are by no means limited to the foregoing scientificreasoning as an explanation for the beneficial anti-angiogenic andtumor-localizing properties of the present antibodies. Although theutility of the invention is self-evident and needs no underlying theoryto be put into practice, the inventors have considered alternativemechanisms by which VEGFR2-blocking, non-VEGFR1-blocking antibodies mayeffectively and specifically localize to tumor vasculature.

Such antibodies could bind to VEGF that is associated with Npn-l oranother, as yet, uncharacterized VEGF binding protein on the cellsurface or could bind VEGF that is bound to heparan sulfateproteoglycans on the surface of endothelial cells. Antibody localizationcould also be enhanced by binding to another member of the VEGF familyof proteins, i.e., VEGF-B, VEGF-C, VEGF-D , which are associated withthe blood vessels, although this is less likely.

Another advantageous property of the VEGFR2-blocking, anti-VEGF or 2C3antibodies of the invention is that these antibodies neutralize thesurvival signal or “protective effect” of VEGF, which is mediatedthrough VEGFR2. In addition to making the antibodies more effectivethemselves, this property makes them particularly useful in combinationwith other agents that are hampered by VEGF's survival function.

For example, VEGF protects the endothelium from radiotherapy. Therefore,both the naked antibodies and immunoconjugates of the present inventionare ideal for use in combination with radiotherapy. Even more benefitsare provided by the use of such an antibody attached to aradiotherapeutic agent. This type of construct would have the tripleadvantages of: (1) exerting an anti-angiogenic effect through theantibody portion; (2) exerting a tumor vasculature destructive effectthrough delivery of the radiotherapeutic agent; and (3) preventingVEGF's typical survival signal from counteracting the effects of theradiotherapeutic agent.

Other constructs with similarly synergistic effects are VEGFR2-blocking,anti-VEGF antibodies in association with anti-tubulin drugs or prodrugs,anti-apoptopic agents and other anti-angiogenic agents. The actions ofagents or drugs that cause apoptosis are antagonized by VEGF. Thepresent invention therefore improves the effectiveness of such agents byneutralizing VEGF. VEGF survival signals also oppose endostatin,limiting this therapy. Therefore, in combined use with endostatin, theVEGFR2-blocking, anti-VEGF or 2C3 antibodies of the invention willneutralize VEGF and amplify the anti-tumor effects of endostatin. 2C3 orother VEGFR2-blocking, anti-VEGF antibodies may also be used tospecifically delivery collagenase to the tumor, where the collagenasewill produce endostatin in situ, achieving similar benefits.

In all such enhanced or synergistic combinations, the antibodies andother agents may be administered separately, or the second agents may belinked to the antibodies for specific delivery (i.e., targeted deliveryto VEGFR1). In combinations with endostatin, chemical conjugates orrecombinant fusion proteins will be preferred, as these will counteractthe short half life of endostatin, which is currently a limitation ofpotential endostatin therapy. Combinations with, or targeted forms of,tissue plasminogen activator (tPA) may also be employed.

Further advantages of the therapeutics of the present invention includethe ability to lower the interstitial pressure. As VEGF-mediatedincreased permeability contributes to the interstitial pressure, reducedsignaling via VEFR2 will reduce both permeability and interstitialpressure. This, in turn, will reduce the barrier to drugs traversing theentirety of the tumor tissue, so that tumor cells distant from thevasculature can be killed. Prolonged therapy can also be achieved as thepresent compositions with have no, negligible or low immunogenicity.

B3. 2C3 Antibody CDR Sequences

The term “variable”, as used herein in reference to antibodies, meansthat certain portions of the variable domains differ extensively insequence among antibodies, and are used in the binding and specificityof each particular antibody to its particular antigen. However, thevariability is not evenly distributed throughout the variable domains ofantibodies. It is concentrated in three segments termed “hypervariableregions”, both in the light chain and the heavy chain variable domains.

The more highly conserved portions of variable domains are called theframework region (FR). The variable domains of native heavy and lightchains each comprise four FRs (FR1, FR2, FR3 and FR4, respectively),largely adopting a β-sheet configuration, connected by threehypervariable regions, which form loops connecting, and in some cases,forming part of, the β-sheet structure.

The hypervariable regions in each chain are held together in closeproximity by the FRs and, with the hypervariable regions from the otherchain, contribute to the formation of the antigen-binding site ofantibodies (Kabat et al., 1991, specifically incorporated herein byreference). The constant domains are not involved directly in binding anantibody to an antigen, but exhibit various effector functions, such asparticipation of the antibody in antibody-dependent cellular toxicity.

The term “hypervariable region”, as used herein, refers to the aminoacid residues of an antibody that are responsible for antigen-binding.The hypervariable region comprises amino acid residues from a“complementarity determining region” or “CDR” (i.e. residues 24-34 L1),50-56 (L2) and 89-97 (L3) in the light chain variable domain and 31-35(H1), 50-56 (H2) and 95-102 (H3) in the heavy chain variable domain;Kabat et al., 1991, specifically incorporated herein by reference)and/or those residues from a “hypervariable loop” (i.e. residues 26-32L1), 50-52(L2) and 91-96 (L3) in the light chain variable domain and26-32 (H1), 53-55 (H2) and 96-101 (H3) in the heavy chain variabledomain). “Framework” or “FR” residues are those variable domain residuesother than the hypervariable region residues as herein defined.

The DNA and deduced amino acid sequences of the Vh and VK chains of the2C3 ScFv fragment are provided herein as SEQ ID NO:6, 7, 8 and 9. Thesesequences encompass CDR1-3 of the variable regions of the heavy andlight chains of the antibody.

As described herein (Section C3), with the provision of structural andfunctional information for a biological molecule, a range of equivalent,or even improved molecules can be generated. This applies to theVEGFR2-blocking, anti-VEGF antibodies of the present invention, asexemplified by 2C3 antibodies. Although antigen-binding and otherfunctional properties of an antibody must be conserved, there is anextremely high degree of skill in the art in making equivalent and evenimproved antibodies once a reference antibody has been provided. Suchtechnical skill can, in light of the sequences and information providedherein, be applied to the production of further antibodies that havelike, improved or otherwise desirable characteristics.

For equivalent antibodies, certain amino acids may substituted for otheramino acids in the antibody constant or variable domain frameworkregions without appreciable loss of interactive binding capacity. It ispreferably that such changes be made in the DNA sequences encoding theantibody portions and that the changes be conservative in nature (seeSection C3, the codon information in Table A, and the supportingtechnical details on site-specific mutagenesis). Naturally, there is alimit to the number of changes that should be made, but this will beknown those of ordinary skill in the art.

Other types of variants are antibodies with improved biologicalproperties relative to the parent antibody from which they aregenerated. Such variants, or second generation compounds, are typicallysubstitutional variants involving one or more substituted hypervariableregion residues of a parent antibody. A convenient way for generatingsuch substitutional variants is affinity maturation using phage display.

In affinity maturation using phage display, several hypervariable regionsites (e.g. 6-7 sites) are mutated to generate all possible aminosubstitutions at each site. The antibody variants thus generated aredisplayed in a monovalent fashion from filamentous phage particles asfusions to the gene III product of M13 packaged within each particle.The phage-displayed variants are then screened for their biologicalactivity (e.g. binding affinity) as herein disclosed. In order toidentify candidate hypervariable region sites for modification, alaninescanning mutagenesis can be performed to identified hypervariable regionresidues contributing significantly to antigen binding.

Alternatively, or in addition, it is contemplated that the crystalstructure of the antigen-antibody complex be delineated and analyzed toidentify contact points between the antibody and VEGF. Such contactresidues and neighboring residues are candidates for substitution. Oncesuch variants are generated, the panel of variants is subjected toscreening, as described herein, and antibodies with analogues butdifferent or even superior properties in one or more relevant assays areselected for further development.

Further aspects of the invention therefore concern isolated DNA segmentsand recombinant vectors encoding CDR regions of VEGFR2-blocking,anti-VEGF antibody heavy and light chains, such as 2C3 heavy and lightchains, and the creation and use of recombinant host cells through theapplication of DNA technology, that express such CDR regions.

The present invention thus concerns DNA segments, isolatable from anymammal, preferably, human or murine, that are free from total genomicDNA and are capable of expressing CDR regions of VEGFR2-blocking,anti-VEGF antibody heavy and light chains, such as 2C3 heavy and lightchains. As used herein, the term “DNA segment” refers to a DNA moleculethat has been isolated free of total genomic DNA of a particularspecies. Included within the term “DNA segment”, are DNA segments andsmaller fragments of such segments, and also recombinant vectors,including, for example, plasmids, cosmids, phage, viruses, and the like.

Similarly, a DNA segment comprising a coding segment or isolated geneportion encoding purified CDR regions of VEGFR2-blocking, anti-VEGFantibody heavy and light chains, such as 2C3 heavy and light chains,refers to a DNA segment including such coding sequences and, in certainaspects, regulatory sequences, isolated substantially away from othernaturally occurring genes or protein encoding sequences. In thisrespect, the term “gene” is used for simplicity to refer to a functionalprotein, polypeptide or peptide encoding unit. As will be understood bythose in the art, this functional term includes the nativeantibody-encoding sequences and smaller engineered segments thatexpress, or may be adapted to express, suitable antigen bindingproteins, polypeptides or peptides.

“Isolated substantially away from other coding sequences” means that thecoding segment or isolated gene portion of interest forms thesignificant part of the coding region of the DNA segment, and that theDNA segment does not contain large portions of naturally-occurringcoding DNA, such as large chromosomal fragments or other functionalgenes or cDNA coding regions. Of course, this refers to the DNA segmentas originally isolated, and does not exclude genes or coding regionslater added to the segment by the hand of man.

In particular embodiments, the invention concerns isolated codingsegments or isolated gene portions and recombinant vectors incorporatingDNA sequences that encode CDR regions of VEGFR2-blocking, anti-VEGFantibody heavy and light chains, such as 2C3 heavy and light chains,that comprise at least a first sequence region that includes an aminoacid sequence region of at least about 75%, more preferably, at leastabout 80%, more preferably, at least about 85%, more preferably, atleast about 90% and most preferably, at least about 95% or so amino acidsequence identity to the amino acid sequence of SEQ ID NO:7 or SEQ IDNO:9; wherein said CDR regions at least substantially maintain thebiological properties of the CDR regions of amino acid sequences SEQ IDNO:7 or SEQ ID NO:9.

As disclosed herein, the sequences may comprise certain biologicallyfunctional equivalent amino acids or “conservative substitutions”. Othersequences may comprise functionally non-equivalent amino acids or“non-conservative substitutions” deliberately engineered to improve theproperties of the CDR or antibody containing the CDR, as is known thoseof ordinary skill in the art and further described herein.

It will also be understood that amino acid and nucleic acid sequencesmay include additional residues, such as additional N- or C-terminalamino acids or 5′ or 3′ sequences, and yet still correspond to asequence of the invention, so long as the sequence meets the criteriaset forth above, preferably including the maintenance or improvement ofbiological protein activity where protein expression is concerned. Theaddition of terminal sequences includes various non-coding sequencesflanking either of the 5′ or 3′ portions of the coding region, and alsocontrol regions.

The nucleic acid segments of the present invention may thus be combinedwith other DNA sequences, such as promoters, polyadenylation signals,additional restriction enzyme sites, multiple cloning sites, othercoding segments, and the like, such that their overall length may varyconsiderably. It is therefore contemplated that a nucleic acid fragmentof almost any length may be employed, with the total length preferablybeing limited by the ease of preparation and use in the intendedrecombinant DNA protocol.

Recombinant vectors therefore form further aspects of the presentinvention. Particularly useful vectors are contemplated to be thosevectors in which the coding portion of the DNA segment is positionedunder the control of a promoter. Generally, although not exclusively, arecombinant or heterologous promoter will be employed, i.e., a promoternot normally associated with coding sequences in their naturalenvironment. Such promoters may include bacterial, viral, eukaryotic andmammalian promoters, so long as the promoter effectively directs theexpression of the DNA segment in the cell type, organism, or evenanimal, chosen for expression.

The use of promoter and cell type combinations for protein expression isknown to those of skill in the art of molecular biology. The promotersemployed may be constitutive, or inducible, and can be used under theappropriate conditions to direct high level expression of the introducedDNA segment, such as is advantageous in the large-scale production ofrecombinant proteins or peptides.

The expression of the nucleic acid sequences of the invention may beconveniently achieved by any one or more standard techniques known thoseof ordinary skill in the art and further described herein. For example,the later description of the recombinant expression of fusion proteinsapplies equally well to antibodies and antibody fragments that are notoperatively associated with another coding sequence at the nucleic acidlevel.

B4. Polyclonal Antibodies

Means for preparing and characterizing antibodies are well known in theart (see, e.g., Antibodies: A Laboratory Manual, Cold Spring HarborLaboratory, 1988; incorporated herein by reference). To preparepolyclonal antisera an animal is immunized with an immunogenic VEGFcomposition, and antisera collected from that immunized animal. A widerange of animal species can be used for the production of antisera.Typically the animal used for production of anti-antisera is a rabbit,mouse, rat, hamster, guinea pig or goat. Because of the relatively largeblood volume of rabbits, a rabbit is a preferred choice for productionof polyclonal antibodies.

The amount of VEGF immunogen composition used in the production ofpolyclonal antibodies varies upon the nature of the immunogen as well asthe animal used for immunization. A variety of routes can be used toadminister the present VEGF immunogen; subcutaneous, intramuscular,intradermal, intravenous, intraperitoneal and intrasplenic. Theproduction of polyclonal antibodies may be monitored by sampling bloodof the immunized animal at various points following immunization. Asecond, booster injection, may also be given. The process of boostingand titering is repeated until a suitable titer is achieved. When adesired titer level is obtained, the immunized animal can be bled andthe serum isolated and stored. The animal can also be used to generatemonoclonal antibodies.

As is well known in the art, the immunogenicity of a particularcomposition can be enhanced by the use of non-specific stimulators ofthe immune response, known as adjuvants. Exemplary adjuvants includecomplete Freund's adjuvant, a non-specific stimulator of the immuneresponse containing killed Mycobacterium tuberculosis; incompleteFreund's adjuvant; and aluminum hydroxide adjuvant.

It may also be desired to boost the host immune system, as may beachieved by associating VEGF with, or coupling VEGF to, a carrier.Exemplary carriers are keyhole limpet hemocyanin (KLH) and bovine serumalbumin (BSA). Other albumins such as ovalbumin, mouse serum albumin orrabbit serum albumin can also be used as carriers. As is also known inthe art, a given composition may vary in its immunogenicity. However,the generation of antibodies against VEGF is not particularly difficult.

B5. Monoclonal Antibodies

Various methods for generating monoclonal antibodies (MAbs) are also nowvery well known in the art. The most standard monoclonal antibodygeneration techniques generally begin along the same lines as those forpreparing polyclonal antibodies (Antibodies: A Laboratory Manual, ColdSpring Harbor Laboratory, 1988; incorporated herein by reference). Apolyclonal antibody response is initiated by immunizing an animal withan immunogenic VEGF composition and, when a desired titer level isobtained, the immunized animal can be used to generate MAbs.

MAbs may be readily prepared through use of well-known techniques, suchas those exemplified in U.S. Pat. No. 4,196,265, incorporated herein byreference. Typically, this technique involves immunizing a suitableanimal with the selected VEGF imnmnunogen composition. The immunizingcomposition is administered in a manner effective to stimulateantibody-producing cells. Rodents such as mice and rats are preferredanimals, however, the use of rabbit, sheep and frog cells is alsopossible. The use of rats may provide certain advantages (Goding, 1986,pp. 60-61; incorporated herein by reference), but mice are preferred,with the BALB/c mouse being most preferred as this is most routinelyused and generally gives a higher percentage of stable fusions.

Following immunization, somatic cells with the potential for producingVEGF antibodies, specifically B lymphocytes (B cells), are selected foruse in the mAb generating protocol. These cells may be obtained frombiopsied spleens, tonsils or lymph nodes, or from a peripheral bloodsample. Spleen cells and peripheral blood cells are preferred, theformer because they are a rich source of antibody-producing cells thatare in the dividing plasmablast stage, and the latter because peripheralblood is easily accessible. Often, a panel of animals will have beenimmunized and the spleen of animal with the highest antibody titer willbe removed and the spleen lymphocytes obtained by homogenizing thespleen with a syringe. Typically, a spleen from an immunized mousecontains approximately 5×10⁷ to 2×10⁸ lymphocytes.

The anti-VEGF antibody-producing B lymphocytes from the immunized animalare then fused with cells of an immortal myeloma cell, generally one ofthe same species as the animal that was immunized. Myeloma cell linessuited for use in hybridoma-producing fusion procedures preferably arenon-antibody-producing, have high fusion efficiency, and enzymedeficiencies that render then incapable of growing in certain selectivemedia which support the growth of only the desired fused cells(hybridomas).

Any one of a number of myeloma cells may be used, as are known to thoseof skill in the art (Goding, pp. 65-66, 1986; Campbell, pp. 75-83, 1984;each incorporated herein by reference). For example, where the immunizedanimal is a mouse, one may use P3-X63/Ag8, X63-Ag8.653, NS1/1.Ag 4 1,Sp210-Agl4, FO, NSO/U, MPC-11, MPC11-X45-GTG 1.7 and S194/5XX0 Bul; forrats, one may use R210. RCY3, Y3-Ag 1.2.3, IR983F, 4B210 or one of theabove listed mouse cell lines; and U-266, GM1500-GRG2, LICR-LON-HMy2 andUC729-6, are all useful in connection with human cell fusions.

Methods for generating hybrids of antibody-producing spleen or lymphnode cells and myeloma cells usually comprise mixing somatic cells withmyeloma cells in a 4:1 proportion, though the proportion may vary fromabout 20:1 to about 1:1, respectively, in the presence of an agent oragents (chemical or electrical) that promote the fusion of cellmembranes. Fusion methods using Sendai virus have been described byKohler and Milstein (1975; 1976; each incorporated herein by reference),and those using polyethylene glycol (PEG), such as 37% (v/v) PEG, byGefter et al. (1977; incorporated herein by reference). The use ofelectrically induced fusion methods is also appropriate (Goding pp.71-74, 1986; incorporated herein by reference).

Fusion procedures usually produce viable hybrids at low frequencies,about 1×10⁻⁶ to 1×10⁻⁸. However, this does not pose a problem, as theviable, fused hybrids are differentiated from the parental, unfusedcells (particularly the unfused myeloma cells that would normallycontinue to divide indefinitely) by culturing in a selective medium. Theselective medium is generally one that contains an agent that blocks thede novo synthesis of nucleotides in the tissue culture media. Exemplaryand preferred agents are aminopterin, methotrexate, and azaserine.Aminopterin and methotrexate block de novo synthesis of both purines andpyrimidines, whereas azaserine blocks only purine synthesis. Whereaminopterin or methotrexate is used, the media is supplemented withhypoxanthine and thymidine as a source of nucleotides (HAT medium).Where azaserine is used, the media is supplemented with hypoxanthine.

The preferred selection medium is HAT. Only cells capable of operatingnucleotide salvage pathways are able to survive in HAT medium. Themyeloma cells are defective in key enzymes of the salvage pathway, e.g.,hypoxanthine phosphoribosyl transferase (HPRT), and they cannot survive.The B cells can operate this pathway, but they have a limited life spanin culture and generally die within about two weeks. Therefore, the onlycells that can survive in the selective media are those hybrids formedfrom myeloma and B cells.

This culturing provides a population of hybridomas from which specifichybridomas are selected. Typically, selection of hybridomas is performedby culturing the cells by single-clone dilution in microtiter plates,followed by testing the individual clonal supernatants (after about twoto three weeks) for the desired anti-VEGF reactivity. The assay shouldbe sensitive, simple and rapid, such as radioimmunoassays, enzymeimmunoassays, cytotoxicity assays, plaque assays, dot immunobindingassays, and the like.

The selected hybridomas would then be serially diluted and cloned intoindividual anti-VEGF antibody-producing cell lines, which clones canthen be propagated indefinitely to provide MAbs. The cell lines may beexploited for mAb production in two basic ways. A sample of thehybridoma can be injected (often into the peritoneal cavity) into ahistocompatible animal of the type that was used to provide the somaticand myeloma cells for the original fusion. The injected animal developstumors secreting the specific monoclonal antibody produced by the fusedcell hybrid. The body fluids of the animal, such as serum or ascitesfluid, can then be tapped to provide MAbs in high concentration. Theindividual cell lines could also be cultured in vitro, where the MAbsare naturally secreted into the culture medium from which they can bereadily obtained in high concentrations.

MAbs produced by either means will generally be further purified, e.g.,using filtration, centrifugation and various chromatographic methods,such as HPLC or affinity chromatography, all of which purificationtechniques are well known to those of skill in the art. Thesepurification techniques each involve fractionation to separate thedesired antibody from other components of a mixture. Analytical methodsparticularly suited to the preparation of antibodies include, forexample, protein A-Sepharose and/or protein G-Sepharose chromatography.

B6. Antibodies from Phagemid Libraries

Recombinant technology now allows the preparation of antibodies havingthe desired specificity from recombinant genes encoding a range ofantibodies (Van Dijk et al., 1989; incorporated herein by reference).Certain recombinant techniques involve the isolation of the antibodygenes by immunological screening of combinatorial immunoglobulin phageexpression libraries prepared from RNA isolated from the spleen of animmunized animal (Morrison et al., 1986; Winter and Milstein, 1991; eachincorporated herein by reference).

For such methods, combinatorial immunoglobulin phagemid libraries areprepared from RNA isolated from the spleen of the immunized animal, andphagemids expressing appropriate antibodies are selected by panningusing cells expressing the antigen and control cells. The advantages ofthis approach over conventional hybridoma techniques are thatapproximately 10⁴ times as many antibodies can be produced and screenedin a single round, and that new specificities are generated by H and Lchain combination, which further increases the percentage of appropriateantibodies generated.

One method for the generation of a large repertoire of diverse antibodymolecules in bacteria utilizes the bacteriophage lambda as the vector(Huse et al., 1989; incorporated herein by reference). Production ofantibodies using the lambda vector involves the cloning of heavy andlight chain populations of DNA sequences into separate starting vectors.The vectors are subsequently combined randomly to form a single vectorthat directs the co-expression of heavy and light chains to formantibody fragments. The heavy and light chain DNA sequences are obtainedby amplification, preferably by PCR™ or a related amplificationtechnique, of mRNA isolated from spleen cells (or hybridomas thereof)from an animal that has been immunized with a selected antigen. Theheavy and light chain sequences are typically amplified using primersthat incorporate restriction sites into the ends of the amplified DNAsegment to facilitate cloning of the heavy and light chain segments intothe starting vectors.

Another method for the generation and screening of large libraries ofwholly or partially synthetic antibody combining sites, or paratopes,utilizes display vectors derived from filamentous phage such as M13, fior fd. These filamentous phage display vectors, referred to as“phagemids”, yield large libraries of monoclonal antibodies havingdiverse and novel immunospecificities. The technology uses a filamentousphage coat protein membrane anchor domain as a means for linkinggene-product and gene during the assembly stage of filamentous phagereplication, and has been used for the cloning and expression ofantibodies from combinatorial libraries (Kang et al., 1991; Barbas etal., 1991; each incorporated herein by reference).

This general technique for filamentous phage display is described inU.S. Pat. No. 5,658,727, incorporated herein by reference. In a mostgeneral sense, the method provides a system for the simultaneous cloningand screening of pre-selected ligand-binding specificities from antibodygene repertoires using a single vector system. Screening of isolatedmembers of the library for a pre-selected ligand-binding capacity allowsthe correlation of the binding capacity of an expressed antibodymolecule with a convenient means to isolate the gene that encodes themember from the library.

Linkage of expression and screening is accomplished by the combinationof targeting of a fusion polypeptide into the periplasm of a bacterialcell to allow assembly of a functional antibody, and the targeting of afusion polypeptide onto the coat of a filamentous phage particle duringphage assembly to allow for convenient screening of the library memberof interest. Periplasmic targeting is provided by the presence of asecretion signal domain in a fusion polypeptide. Targeting to a phageparticle is provided by the presence of a filamentous phage coat proteinmembrane anchor domain (i.e., a cpIII- or cpVIII-derived membrane anchordomain) in a fusion polypeptide.

The diversity of a filamentous phage-based combinatorial antibodylibrary can be increased by shuffling of the heavy and light chaingenes, by altering one or more of the complementarity determiningregions of the cloned heavy chain genes of the library. or byintroducing random mutations into the library by error-prone polymerasechain reactions. Additional methods for screening phagemid libraries aredescribed in U.S. Pat. Nos. 5,580,717; 5,427,908; 5,403,484; and5,223,409, each incorporated herein by reference.

Another method for the screening of large combinatorial antibodylibraries has been developed, utilizing expression of populations ofdiverse heavy and light chain sequences on the surface of a filamentousbacteriophage, such as M13, fl or fd (U.S. Pat. No. 5,698,426;incorporated herein by reference). Two populations of diverse heavy (Hc)and light (Lc) chain sequences are synthesized by polymerase chainreaction (PCR™). These populations are cloned into separate M13-basedvector containing elements necessary for expression. The heavy chainvector contains a gene VIII (gVIII) coat protein sequence so thattranslation of the heavy chain sequences produces gVIII-Hc fusionproteins. The populations of two vectors are randomly combined such thatonly the vector portions containing the Hc and Lc sequences are joinedinto a single circular vector.

The combined vector directs the co-expression of both Hc and Lcsequences for assembly of the two polypeptides and surface expression onM13 (U.S. Pat. No. 5,698,426; incorporated herein by reference). Thecombining step randomly brings together different Hc and Lc encodingsequences within two diverse populations into a single vector. Thevector sequences donated from each independent vector are necessary forproduction of viable phage. In addition, since the pseudo gVIIIsequences are contained in only one of the two starting vectors,co-expression of functional antibody fragments as Lc associated gVIII-Hcfusion proteins cannot be accomplished on the phage surface until thevector sequences are linked in the single vector.

Surface expression of the antibody library is performed in an ambersuppressor strain. An amber stop codon between the Hc sequence and thegVIII sequence unlinks the two components in a non-suppressor strain.Isolating the phage produced from the non-suppressor strain andinfecting a suppressor strain will link the Hc sequences to the gVIIIsequence during expression. Culturing the suppressor strain afterinfection allows the coexpression on the surface of M13 of all antibodyspecies within the library as gVIII fusion proteins (gVIII-Fab fusionproteins). Alternatively, the DNA can be isolated from thenon-suppressor strain and then introduced into a suppressor strain toaccomplish the same effect.

The surface expression library is screened for specific Fab fragmentsthat bind preselected molecules by standard affinity isolationprocedures. Such methods include, for example, panning (Parmley andSmith, 1988; incorporated herein by reference), affinity chromatographyand solid phase blotting procedures. Panning is preferred, because hightiters of phage can be screened easily, quickly and in small volumes.Furthermore, this procedure can select minor Fab fragments specieswithin the population, which otherwise would have been undetectable, andamplified to substantially homogenous populations. The selected Fabfragments can be characterized by sequencing the nucleic acids encodingthe polypeptides after amplification of the phage population.

Another method for producing diverse libraries of antibodies andscreening for desirable binding specificities is described in U.S. Pat.No. 5,667,988 and U.S. Pat. No. 5,759,817, each incorporated herein byreference. The method involves the preparation of libraries ofheterodimeric immunoglobulin molecules in the form of phagemid librariesusing degenerate oligonucleotides and primer extension reactions toincorporate the degeneracies into the CDR regions of the immunoglobulinvariable heavy and light chain variable domains, and display of themutagenized polypeptides on the surface of the phagemid. Thereafter, thedisplay protein is screened for the ability to bind to a preselectedantigen.

The method for producing a heterodimeric immunoglobulin moleculegenerally involves (1) introducing a heavy or light chain Vregion-coding gene of interest into the phagemid display vector; (2)introducing a randomized binding site into the phagemid display proteinvector by primer extension with an oligonucleotide containing regions ofhomology to a CDR of the antibody V region gene and containing regionsof degeneracy for producing randomized coding sequences to form a largepopulation of display vectors each capable of expressing differentputative binding sites displayed on a phagemid surface display protein;(3) expressing the display protein and binding site on the surface of afilamentous phage particle; and (4) isolating (screening) thesurface-expressed phage particle using affinity techniques such aspanning of phage particles against a preselected antigen, therebyisolating one or more species of phagemid containing a display proteincontaining a binding site that binds a preselected antigen.

A further variation of this method for producing diverse libraries ofantibodies and screening for desirable binding specificities isdescribed in U.S. Pat. No. 5,702,892, incorporated herein by reference.In this method, only heavy chain sequences are employed, the heavy chainsequences are randomized at all nucleotide positions which encode eitherthe CDRI or CDRIII hypervariable region, and the genetic variability inthe CDRs is generated independent of any biological process.

In the method, two libraries are engineered to genetically shuffleoligonucleotide motifs within the framework of the heavy chain genestructure. Through random mutation of either CDRI or CDRIII, thehypervariable regions of the heavy chain gene were reconstructed toresult in a collection of highly diverse sequences. The heavy chainproteins encoded by the collection of mutated gene sequences possessedthe potential to have all of the binding characteristics of animmunoglobulin while requiring only one of the two immunoglobulinchains.

Specifically, the method is practiced in the absence of theimmunoglobulin light chain protein. A library of phage displayingmodified heavy chain proteins is incubated with an immobilized ligand toselect clones encoding recombinant proteins that specifically bind theimmobilized ligand. The bound phage are then dissociated from theimmobilized ligand and amplified by growth in bacterial host cells.Individual viral plaques, each expressing a different recombinantprotein, are expanded, and individual clones can then be assayed forbinding activity.

B7. Antibodies from Human Lymphocytes

In vitro immunization, or antigen stimulation, may also be used togenerate a human anti-VEGF antibody. Such techniques can be used tostimulate peripheral blood lymphocytes from normal, healthy subjects,simply by stimulating antibody-producing cells with VEGF in vitro.

Such “in vitro immunization” involves antigen-specific activation ofnon-immunized B lymphocytes, generally within a mixed population oflymphocytes (mixed lymphocyte cultures, MLC). In vitro immunizations mayalso be supported by B cell growth and differentiation factors andlymphokines. The antibodies produced by these methods are often IgMantibodies (Borrebaeck et al., 1986; incorporated herein by reference).

Another method has been described (U.S. Pat. No. 5,681,729, incorporatedherein by reference) wherein human lymphocytes that mainly produce IgG(or IgA) antibodies can be obtained. The method involves, in a generalsense, transplanting human lymphocytes to an immunodeficient animal sothat the human lymphocytes “take” in the animal body; immunizing theanimal with a desired antigen, so as to generate human lymphocytesproducing an antibody specific to the antigen; and recovering the humanlymphocytes producing the antibody from the animal. The humanlymphocytes thus produced can be used to produce a monoclonal antibodyby immortalizing the human lymphocytes producing the antibody, cloningthe obtained immortalized human-originated lymphocytes producing theantibody, and recovering a monoclonal antibody specific to the desiredantigen from the cloned immortalized human-originated lymphocytes.

The immunodeficient animals that may be employed in this technique arethose that do not exhibit rejection when human lymphocytes aretransplanted to the animals. Such animals may be artificially preparedby physical, chemical or biological treatments. Any immunodeficientanimal may be employed. The human lymphocytes may be obtained from humanperipheral blood, spleen, lymph nodes, tonsils or the like.

The “taking” of the transplanted human lymphocytes in the animals can beattained by merely administering the human lymphocytes to the animals.The administration route is not restricted and may be, for example,subcutaneous, intravenous or intraperitoneal. The dose of the humanlymphocytes is not restricted, and can usually be 10⁶ to 10⁸ lymphocytesper animal. The immunodeficient animal is then immunized with thedesired VEGF antigen.

After the immunization, human lymphocytes are recovered from the blood,spleen, lymph nodes or other lymphatic tissues by any conventionalmethod. For example, mononuclear cells can be separated by theFicoll-Hypaque (specific gravity: 1.077) centrifugation method, and themonocytes removed by the plastic dish adsorption method. Thecontaminating cells originating from the immunodeficient animal may beremoved by using an antiserum specific to the animal cells. Theantiserum may be obtained by, for example, immunizing a second, distinctanimal with the spleen cells of the immunodeficient animal, andrecovering serum from the distinct immunized animal. The treatment withthe antiserum may be carried out at any stage. The human lymphocytes mayalso be recovered by an immunological method employing a humanimmunoglobulin expressed on the cell surface as a marker.

By these methods, human lymphocytes mainly producing IgG and IgAantibodies specific to one or more selected VEGF epitopes can beobtained. Monoclonal antibodies are then obtained from the humanlymphocytes by immortalization, selection, cell growth and antibodyproduction.

B8. Transgenic Mice Containing Human Antibody Libraries

Recombinant technology is now available for the preparation ofantibodies. In addition to the combinatorial immunoglobulin phageexpression libraries disclosed above, another molecular cloning approachis to prepare antibodies from transgenic mice containing human antibodylibraries. Such techniques are described in U.S. Pat. No. 5,545,807,incorporated herein by reference.

In a most general sense, these methods involve the production of atransgenic animal that has inserted into its germline genetic materialthat encodes for at least part of an immunoglobulin of human origin orthat can rearrange to encode a repertoire of immunoglobulins. Theinserted genetic material may be produced from a human source, or may beproduced synthetically. The material may code for at least part of aknown immunoglobulin or may be modified to code for at least part of analtered immunoglobulin.

The inserted genetic material is expressed in the transgenic animal,resulting in production of an immunoglobulin derived at least in partfrom the inserted human immunoglobulin genetic material. It is found thegenetic material is rearranged in the transgenic animal, so that arepertoire of immunoglobulins with part or parts derived from insertedgenetic material may be produced, even if the inserted genetic materialis incorporated in the germline in the wrong position or with the wronggeometry.

The inserted genetic material may be in the form of DNA cloned intoprokaryotic vectors such as plasmids and/or cosmids. Larger DNAfragments are inserted using yeast artificial chromosome vectors (Burkeet al., 1987; incorporated herein by reference). or by introduction ofchromosome fragments (Richer and Lo, 1989; incorporated herein byreference). The inserted genetic material may be introduced to the hostin conventional manner, for example by injection or other proceduresinto fertilized eggs or embryonic stem cells.

In preferred aspects, a host animal that initially does not carrygenetic material encoding immunoglobulin constant regions is utilized,so that the resulting transgenic animal will use only the inserted humangenetic material when producing immunoglobulins. This can be achievedeither by using a naturally occurring mutant host lacking the relevantgenetic material, or by artificially making mutants e.g., in cell linesultimately to create a host from which the relevant genetic material hasbeen removed.

Where the host animal carries genetic material encoding immunoglobulinconstant regions, the transgenic animal will carry the naturallyoccurring genetic material and the inserted genetic material and willproduce immunoglobulins derived from the naturally occurring geneticmaterial, the inserted genetic material, and mixtures of both types ofgenetic material. In this case the desired immunoglobulin can beobtained by screening hybridomas derived from the transgenic animal,e.g., by exploiting the phenomenon of allelic exclusion of antibody geneexpression or differential chromosome loss.

Once a suitable transgenic animal has been prepared, the animal issimply immunized with the desired immunogen. Depending on the nature ofthe inserted material, the animal may produce a chimeric immunoglobulin,e.g. of mixed mouse/human origin, where the genetic material of foreignorigin encodes only part of the immunoglobulin; or the animal mayproduce an entirely foreign immunoglobulin, e.g. of wholly human origin,where the genetic material of foreign origin encodes an entireimmunoglobulin.

Polyclonal antisera may be produced from the transgenic animal followingimmunization. Immunoglobulin-producing cells may be removed from theanimal to produce the immunoglobulin of interest. Preferably, monoclonalantibodies are produced from the transgenic animal, e.g., by fusingspleen cells from the animal with myeloma cells and screening theresulting hybridomas to select those producing the desired antibody.Suitable techniques for such processes are described herein.

In an alternative approach, the genetic material may be incorporated inthe animal in such a way that the desired antibody is produced in bodyfluids such as serum or external secretions of the animal, such as milk,colostrum or saliva. For example, by inserting in vitro genetic materialencoding for at least part of a human immunoglobulin into a gene of amammal coding for a milk protein and then introducing the gene to afertilized egg of the mammal, e.g., by injection, the egg may developinto an adult female mammal producing milk containing immunoglobulinderived at least in part from the inserted human immunoglobulin geneticmaterial. The desired antibody can then be harvested from the minkSuitable techniques for carrying out such processes are known to thoseskilled in the art.

The foregoing transgenic animals are usually employed to produce humanantibodies of a single isotype, more specifically an isotype that isessential for B cell maturation, such as IgM and possibly IgD. Anotherpreferred method for producing human anti-VEGF antibodies is to use thetechnology described in U.S. Pat. Nos. 5,545,806; 5,569,825; 5,625,126;5,633,425; 5,661,016; and 5,770,429; each incorporated by reference,wherein transgenic animals are described that are capable of switchingfrom an isotype needed for B cell development to other isotypes.

In the development of a B lymphocyte, the cell initially produces IgMwith a binding specificity determined by the productively rearrangedV_(H) and V_(L) regions. Subsequently, each B cell and its progeny cellssynthesize antibodies with the same L and H chain V regions, but theymay switch the isotype of the H chain. The use of mu or delta constantregions is largely determined by alternate splicing, permitting IgM andIgD to be coexpressed in a single cell. The other heavy chain isotypes(gamma, alpha, and epsilon) are only expressed natively after a generearrangement event deletes the C mu and C delta exons. This generearrangement process, termed isotype switching, typically occurs byrecombination between so called switch segments located immediatelyupstream of each heavy chain gene (except delta). The individual switchsegments are between 2 and 10 kb in length, and consist primarily ofshort repeated sequences.

For these reasons, it is preferable that transgenes incorporatetranscriptional regulatory sequences within about 1-2 kb upstream ofeach switch region that is to be utilized for isotype switching. Thesetranscriptional regulatory sequences preferably include a promoter andan enhancer element, and more preferably include the 5′ flanking (i.e.,upstream) region that is naturally associated (i.e., occurs in germlineconfiguration) with a switch region. Although a 5′ flanking sequencefrom one switch region can be operably linked to a different switchregion for transgene construction, in some embodiments it is preferredthat each switch region incorporated in the transgene construct have the5′ flanking region that occurs immediately upstream in the naturallyoccurring germline configuration. Sequence information relating toimmunoglobulin switch region sequences is known (Mills et al., 1990;Sideras et al, 1989; each incorporated herein by reference).

In the method described in U.S. Pat. Nos. 5,545,806; 5,569,825;5,625,126; 5,633,425; 5,661,016; and 5,770,429, the human immunoglobulintransgenes contained within the transgenic animal function correctlythroughout the pathway of B-cell development, leading to isotypeswitching. Accordingly, in this method, these transgenes are constructedso as to produce isotype switching and one or more of the following: (1)high level and cell-type specific expression, (2) functional generearrangement, (3) activation of and response to allelic exclusion, (4)expression of a sufficient primary repertoire, (5) signal transduction,(6) somatic hypermutation, and (7) domination of the transgene antibodylocus during the immune response.

An important requirement for transgene function is the generation of aprimary antibody repertoire that is diverse enough to trigger asecondary immune response for a wide range of antigens. The rearrangedheavy chain gene consists of a signal peptide exon, a variable regionexon and a tandem array of multi-domain constant region regions, each ofwhich is encoded by several exons. Each of the constant region genesencode the constant portion of a different class of immunoglobulins.During B-cell development, V region proximal constant regions aredeleted leading to the expression of new heavy chain classes. For eachheavy chain class, alternative patterns of RNA splicing give rise toboth transmembrane and secreted immunoglobulins.

The human heavy chain locus consists of approximately 200 V genesegments spanning 2 Mb, approximately 30 D gene segments spanning about40 kb, six J segments clustered within a 3 kb span, and nine constantregion gene segments spread out over approximately 300 kb. The entirelocus spans approximately 2.5 Mb of the distal portion of the long armof chromosome 14. Heavy chain transgene fragments containing members ofall six of the known V_(H) families, the D and J gene segments, as wellas the mu, delta, gamma 3, gamma 1 and alpha 1 constant regions areknown (Berman et al., 1988; incorporated herein by reference). Genomicfragments containing all of the necessary gene segments and regulatorysequences from a human light chain locus is similarly constructed.

The expression of successfully rearranged immunoglobulin heavy and lighttransgenes usually has a dominant effect by suppressing therearrangement of the endogenous immunoglobulin genes in the tansgenicnonhuman animal. However, in certain embodiments, it is desirable toeffect complete inactivation of the endogenous Ig loci so that hybridimmunoglobulin chains comprising a human variable region and a non-human(e.g., murine) constant region cannot be formed, for example bytrans-switching between the transgene and endogenous Ig sequences. Usingembryonic stem cell technology and homologous recombination, theendogenous immunoglobulin repertoire can be readily eliminated. Inaddition, suppression of endogenous Ig genes may be accomplished using avariety of techniques, such as antisense technology.

In other aspects of the invention, it may be desirable to produce atrans-switched immunoglobulin. Antibodies comprising such chimerictrans-switched immunoglobulins can be used for a variety of applicationswhere it is desirable to have a non-human (e.g., murine) constantregion, e.g., for retention of effector functions in the host. Thepresence of a murine constant region can afford advantages over a humanconstant region, for example, to provide murine effector functions(e.g., ADCC, murine complement fixation) so that such a chimericantibody may be tested in a mouse disease model. Subsequent to theanimal testing, the human variable region encoding sequence may beisolated, e.g., by PCR™ amplification or cDNA cloning from the source(hybridoma clone), and spliced to a sequence encoding a desired humanconstant region to encode a human sequence antibody more suitable forhuman therapeutic use.

B9. Humanized Antibodies

Human antibodies generally have at least three potential advantages foruse in human therapy. First, because the effector portion is human, itmay interact better with the other parts of the human immune system,e.g., to destroy target cells more efficiently by complement-dependentcytotoxicity (CDC) or antibody-dependent cellular cytotoxicity (ADCC).Second, the human immune system should not recognize the antibody asforeign. Third, the half-life in the human circulation will be similarto naturally occurring human antibodies, allowing smaller and lessfrequent doses to be given.

Various methods for preparing human anti-VEGF antibodies are providedherein. In addition to human antibodies, “humanized” antibodies havemany advantages. “Humanized” antibodies are generally chimeric or mutantmonoclonal antibodies from mouse, rat, hamster, rabbit or other species,bearing human constant and/or variable region domains or specificchanges. Techniques for generating a so-called “humanized” anti-VEGFantibody are well known to those of skill in the art.

Humanized antibodies also share the foregoing advantages. First, theeffector portion is still human. Second, the human immune system shouldnot recognize the framework or constant region as foreign, and thereforethe antibody response against such an injected antibody should be lessthan against a totally foreign mouse antibody. Third, injected humanizedantibodies, as opposed to injected mouse antibodies, will presumablyhave a half-life more similar to naturally occurring human antibodies,also allowing smaller and less frequent doses.

A number of methods have been described to produce humanized antibodies.Controlled rearrangement of antibody domains joined through proteindisulfide bonds to form new, artificial protein molecules or “chimeric”antibodies can be utilized (Konieczny et al., 1981; incorporated hereinby reference). Recombinant DNA technology can also be used to constructgene fusions between DNA sequences encoding mouse antibody variablelight and heavy chain domains and human antibody light and heavy chainconstant domains (Morrison et al., 1984; incorporated herein byreference).

DNA sequences encoding the antigen binding portions or complementaritydetermining regions (CDR's) of murine monoclonal antibodies can begrafted by molecular means into the DNA sequences encoding theframeworks of human antibody heavy and light chains (Riechmaun et al.,1988). The expressed recombinant products are called “reshaped” orhumanized antibodies, and comprise the framework of a human antibodylight or heavy chain and the antigen recognition portions, CDR's, of amurine monoclonal antibody.

Another method for producing humanized antibodies is described in U.S.Pat. No. 5,639,641, incorporated herein by reference. The methodprovides, via resurfacing, humanized rodent antibodies that haveimproved therapeutic efficacy due to the presentation of a human surfacein the variable region. In the method: (1) position alignments of a poolof antibody heavy and light chain variable regions is generated to givea set of heavy and light chain variable region framework surface exposedpositions, wherein the alignment positions for all variable regions areat least about 98% identical; (2) a set of heavy and light chainvariable region framework surface exposed amino acid residues is definedfor a rodent antibody (or fragment thereof); (3) a set of heavy andlight chain variable region framework surface exposed amino acidresidues that is most closely identical to the set of rodent surfaceexposed amino acid residues is identified; (4) the set of heavy andlight chain variable region framework surface exposed amino acidresidues defined in step (2) is substituted with the set of heavy andlight chain variable region framework surface exposed amino acidresidues identified in step (3), except for those amino acid residuesthat are within 5A of any atom of any residue of the complementaritydetermining regions of the rodent antibody; and (5) the humanized rodentantibody having binding specificity is produced.

A similar method for the production of humanized antibodies is describedin U.S. Pat. Nos. 5,693,762; 5,693,761; 5,585,089; and 5,530,101, eachincorporated herein by reference. These methods involve producinghumanized immunoglobulins having one or more complementarity determiningregions (CDR's) and possible additional amino acids from a donorimmunoglobulin and a framework region from an accepting humanimmunoglobulin. Each humanized immunoglobulin chain usually comprises,in addition to the CDR's, amino acids from the donor immunoglobulinframework that are capable of interacting with the CDR's to effectbinding affinity, such as one or more amino acids that are immediatelyadjacent to a CDR in the donor immunoglobulin or those within about 3 Åas predicted by molecular modeling. The heavy and light chains may eachbe designed by using any one, any combination, or all of the variousposition criteria described in U.S. Pat. Nos. 5,693,762; 5,693,761;5,585,089; and 5,530,101, each incorporated herein by reference. Whencombined into an intact antibody, the humanized immunoglobulins aresubstantially non-immunogenic in humans and retain substantially thesame affinity as the donor immunoglobulin to the original antigen.

An additional method for producing humanized antibodies is described inU.S. Pat. No. 5,565,332 and 5,733,743, each incorporated herein byreference. This method combines the concept of humanizing antibodieswith the phagemid libraries also described in detail herein. In ageneral sense, the method utilizes sequences from the antigen bindingsite of an antibody or population of antibodies directed against anantigen of interest. Thus for a single rodent antibody, sequencescomprising part of the antigen binding site of the antibody may becombined with diverse repertoires of sequences of human antibodies thatcan, in combination, create a complete antigen binding site.

The antigen binding sites created by this process differ from thosecreated by CDR grafting, in that only the portion of sequence of theoriginal rodent antibody is likely to make contacts with antigen in asimilar manner. The selected human sequences are likely to differ insequence and make alternative contacts with the antigen from those ofthe original binding site. However, the constraints imposed by bindingof the portion of original sequence to antigen and the shapes of theantigen and its antigen binding sites, are likely to drive the newcontacts of the human sequences to the same region or epitope of theantigen. This process has therefore been termed “epitope imprintedselection” (EIS).

Starting with an animal antibody, one process results in the selectionof antibodies that are partly human antibodies. Such antibodies may besufficiently similar in sequence to human antibodies to be used directlyin therapy or after alteration of a few key residues. Sequencedifferences between the rodent component of the selected antibody withhuman sequences could be minimized by replacing those residues thatdiffer with the residues of human sequences, for example, by sitedirected mutagenesis of individual residues, or by CDR grafting ofentire loops. However, antibodies with entirely human sequences can alsobe created. EIS therefore offers a method for making partly human orentirely human antibodies that bind to the same epitope as animal orpartly human antibodies respectively. In EIS, repertoires of antibodyfragments can be displayed on the surface of filamentous phase and thegenes encoding fragments with antigen binding activities selected bybinding of the phage to antigen.

Additional methods for humanizing antibodies contemplated for use in thepresent invention are described in U.S. Pat. Nos. 5,750,078; 5,502,167;5,705,154; 5,770,403; 5,698,417; 5,693,493; 5,558,864; 4,935,496; and4,816,567, each incorporated herein by reference. WO 98/45331 and WO98/45332 are believed to be particularly instructive and areincorporated herein by reference to further exemplify the principles ofhumanization as applied to anti-VEGF antibodies.

B10. Mutagenesis by PCR™

Site-specific mutagenesis is a technique useful in the preparation ofindividual antibodies through specific mutagenesis of the underlyingDNA. The technique further provides a ready ability to prepare and testsequence variants, incorporating one or more of the foregoingconsiderations, whether humanizing or not, by introducing one or morenucleotide sequence changes into the DNA.

Although many methods are suitable for use in mutagenesis, the use ofthe polymerase chain reaction (PCR™) is generally now preferred. Thistechnology offers a quick and efficient method for introducing desiredmutations into a given DNA sequence. The following text particularlydescribes the use of PCR™ to introduce point mutations into a sequence,as may be used to change the amino acid encoded by the given sequence.Adaptations of this method are also suitable for introducing restrictionenzyme sites into a DNA molecule.

In this method, synthetic oligonucleotides are designed to incorporate apoint mutation at one end of an amplified segment. Following PCR™, theamplified fragments are blunt-ended by treating with Klenow fragments,and the blunt-ended fragments are then ligated and subcloned into avector to facilitate sequence analysis.

To prepare the template DNA that one desires to mutagenize, the DNA issubcloned into a high copy number vector, such as pUC19, usingrestriction sites flanking the area to be mutated. Template DNA is thenprepared using a plasmid miniprep. Appropriate oligonucleotide primersthat are based upon the parent sequence, but which contain the desiredpoint mutation and which are flanked at the 5′ end by a restrictionenzyme site, are synthesized using an automated synthesizer. It isgenerally required that the primer be homologous to the template DNA forabout 15 bases or so. Primers may be purified by denaturingpolyacrylamide gel electrophoresis, although this is not absolutelynecessary for use in PCR™. The 5′ end of the oligonucleotides shouldthen be phosphorylated.

The template DNA should be amplified by PCR™, using the oligonucleotideprimers that contain the desired point mutations. The concentration ofMgCl₂ in the amplification buffer will generally be about 15 mM.Generally about 20-25 cycles of PCR™ should be carried out as follows:denaturation, 35 sec. at 95° C.; hybridization, 2 min. at 50° C.; andextension, 2 min. at 72° C. The PCR™ will generally include a last cycleextension of about 10 min. at 72° C. After the final extension step,about 5 units of Klenow fragments should be added to the reactionmixture and incubated for a further 15 min. at about 30° C. Theexonuclease activity of the Klenow fragments is required to make theends flush and suitable for blunt-end cloning.

The resultant reaction mixture should generally be analyzed bynondenaturing agarose or acrylamide gel electrophoresis to verify thatthe amplification has yielded the predicted product. One would thenprocess the reaction mixture by removing most of the mineral oils,extracting with chloroform to remove the remaining oil, extracting withbuffered phenol and then concentrating by precipitation with 100%ethanol. Next, one should digest about half of the amplified fragmentswith a restriction enzyme that cuts at the flanking sequences used inthe oligonucleotides. The digested fragments are purified on a lowgelling/melting agarose gel.

To subclone the fragments and to check the point mutation, one wouldsubclone the two amplified fragments into an appropriately digestedvector by blunt-end ligation. This would be used to transform E. coli,from which plasmid DNA could subsequently be prepared using a miniprep.The amplified portion of the plasmid DNA would then be analyzed by DNAsequencing to confirm that the correct point mutation was generated.This is important as Taq DNA polymerase can introduce additionalmutations into DNA fragments.

The introduction of a point mutation can also be effected usingsequential PCR™ steps. In this procedure, the two fragments encompassingthe mutation are annealed with each other and extended by mutuallyprimed synthesis. This fragment is then amplified by a second PCR™ step,thereby avoiding the blunt-end ligation required in the above protocol.In this method, the preparation of the template DNA, the generation ofthe oligonucleotide primers and the first PCR™ amplification areperformed as described above. In this process, however, the chosenoligonucleotides should be homologous to the template DNA for a stretchof between about 15 and about 20 bases and must also overlap with eachother by about 10 bases or more.

In the second PCR™ amplification, one would use each amplified fragmentand each flanking sequence primer and carry PCR™ for between about 20and about 25 cycles, using the conditions as described above. One wouldagain subclone the fragments and check that the point mutation wascorrect by using the steps outlined above.

In using either of the foregoing methods, it is generally preferred tointroduce the mutation by amplifying as small a fragment as possible. Ofcourse, parameters such as the melting temperature of theoligonucleotide, as will generally be influenced by the GC content andthe length of the oligo, should also be carefully considered. Theexecution of these methods, and their optimization if necessary, will beknown to those of skill in the art and are further described in variouspublications, such as Current Protocols in Molecular Biology, 1995,incorporated herein by reference.

When performing site-specific mutagenesis, Table A can be employed as areference.

TABLE A Amino Acids Codons Alanine Ala A GCA GCC GCG GCU Cysteine Cys CUGC UGU Aspartic acid Asp D GAC GAU Glutamic acid Glu E GAA GAGPhenylalanine Phe F UUC UUU Glycine Gly G GGA GGC GGG GGU Histidine HisH CAC CAU Isoleucine Ile I AUA AUC AUU Lysine Lys K AAA AAG Leucine LeuL UUA UUG CUA CUC CUG CUU Methionine Met M AUG Asparagine Asn N AAC AAUProline Pro P CCA CCC CCG CCU Glutamine Gln Q CAA CAG Arginine Arg R AGAAGG CGA CGC CGG CGU Serine Ser S AGC AGU UCA UCC UCG UCU Threonine Thr TACA ACC ACG ACU Valine Val V GUA GUC GUG GUU Tryptophan Trp W UGGTyrosine Tyr Y UAC UAU

B11. Antibody Fragments and Derivatives

Irrespective of the source of the original VEGFR2-blocking, anti-VEGFantibody, either the intact antibody, antibody multimers, or any one ofa variety of functional, antigen-binding regions of the antibody may beused in the present invention. Exemplary functional regions includediabodies, linear antibodies and scFv, Fv, Fab′, Fab, F(ab′)₂ fragmentsof the anti-VEGF antibodies. Techniques for preparing such constructsare well known to those in the art and are further exemplified herein.

The choice of antibody construct may be influenced by various factors.For example, prolonged half-life can result from the active readsorptionof intact antibodies within the kidney, a property of the Fc piece ofimmunoglobulin. IgG based antibodies, therefore, are expected to exhibitslower blood clearance than their Fab′ counterparts. However, Fab′fragment-based compositions will generally exhibit better tissuepenetrating capability.

Antibody fragments can be obtained by proteolysis of the wholeimmunoglobulin by the non-specific thiol protease, papain. Papaindigestion yields two identical antigen-binding fragments, termed “Fabfragments”, each with a single antigen-binding site, and a residual “Fcfragment”.

Papain must first be activated by reducing the sulfhydryl group in theactive site with cysteine, 2-mercaptoethanol or dithiothreitol. Heavymetals in the stock enzyme should be removed by chelation with EDTA (2mM) to ensure maximum enzyme activity. Enzyme and substrate are normallymixed together in the ratio of 1:100 by weight. After incubation, thereaction can be stopped by irreversible alkylation of the thiol groupwith iodoacetamide or simply by dialysis. The completeness of thedigestion should be monitored by SDS-PAGE and the various fractionsseparated by protein A-Sepharose or ion exchange chromatography.

The usual procedure for preparation of F(ab′)₂ fragments from IgG ofrabbit and human origin is limited proteolysis by the enzyme pepsin. Theconditions, 100x antibody excess w/w in acetate buffer at pH 4.5, 37°C., suggest that antibody is cleaved at the C-terminal side of theinter-heavy-chain disulfide bond. Rates of digestion of mouse IgG mayvary with subclass and conditions should be chosen to avoid significantamounts of completely degraded IgG. In particular, IgG_(2b) issusceptible to complete degradation. The other subclasses requiredifferent incubation conditions to produce optimal results, all of whichis known in the art.

Pepsin treatment of intact antibodies yields an F(ab′)₂ fragment thathas two antigen-combining sites and is still capable of cross-linkingantigen. Digestion of rat IgG by pepsin requires conditions includingdialysis in 0.1 M acetate buffer, pH 4.5, and then incubation for fourhours with 1% w/w pepsin; IgG₁ and IgG₂a digestion is improved if firstdialyzed against 0.1 M formate buffer, pH 2.8, at 4° C., for 16 hoursfollowed by acetate buffer. IgG_(2b) gives more consistent results withincubation in staphylococcal V8 protease (3% w/w) in 0.1 M sodiumphosphate buffer, pH 7.8, for four hours at 37° C.

An Fab fragment also contains the constant domain of the light chain andthe first constant domain (CH1) of the heavy chain. Fab′ fragmentsdiffer from Fab fragments by the addition of a few residues at thecarboxyl terminus of the heavy chain CH1 domain including one or morecysteine(s) from the antibody hinge region. F(ab′)₂ antibody fragmentswere originally produced as pairs of Fab′ fragments that have hingecysteines between them. Other chemical couplings of antibody fragmentsare also known.

An “Fv” fragment is the minimum antibody fragment that contains acomplete antigen-recognition and binding site. This region consists of adimer of one heavy chain and one light chain variable domain in tight,con-covalent association. It is in this configuration that the threehypervariable regions of each variable domain interact to define anantigen-binding site on the surface of the V_(H)-V_(L) dimer.Collectively, the six hypervariable regions confer antigen-bindingspecificity to the antibody. However, even a single variable domain (orhalf of an Fv comprising only three hypervariable regions specific foran antigen) has the ability to recognize and bind antigen, although at alower affinity than the entire binding site.

“Single-chain Fv” or “sFv” antibody fragments comprise the V_(H) andV_(L) domains of antibody, wherein these domains are present in a singlepolypeptide chain. Generally, the Fv polypeptide further comprises apolypeptide linker between the V_(H) and V_(L) domains that enables thesFv to form the desired structure for antigen binding.

The following patents and patent applications are specificallyincorporated herein by reference for the purposes of even furthersupplementing the present teachings regarding the preparation and use offunctional, antigen-binding regions of antibodies, including scFv, Fv,Fab′, Fab and F(ab′)₂ fragments of the anti-VEGF antibodies: U.S. Pat.Nos. 5,855,866; 5,965,132; 6,051,230; 6,004,555; and 5,877,289; and U.S.application Ser. No. 08/482,369, Issue Fee Paid Oct. 20, 1998. WO98/45331 is also incorporated herein by reference for purposes includingeven further describing and teaching the preparation of variable,hypervariable and complementarity determining (CDR) regions ofantibodies,

“Diabodies” are small antibody fragments with two antigen-binding sites,which fragments comprise a heavy chain variable domain (V_(H)) connectedto a light chain variable domain (V_(L)) in the same polypeptide chain(V_(H)-V_(L)). By using a linker that is too short to allow pairingbetween the two domains on the same chain, the domains are forced topair with the complementary domains of another chain and create twoantigen-binding sites. Diabodies are described in EP 404,097 and WO93/11161, each specifically incorporated herein by reference. “Linearantibodies”, which can be bispecific or monospecific, comprise a pair oftandem Fd segments (V_(H)-C_(H)1-V_(H)-C_(H)1) that form a pair ofantigen binding regions, as described in Zapata et al. (1995),specifically incorporated herein by reference.

In using a Fab′ or antigen binding fragment of an antibody, with theattendant benefits on tissue penetration, one may derive additionaladvantages from modifying the fragment to increase its half-life. Avariety of techniques may be employed, such as manipulation ormodification of the antibody molecule itself, and also conjugation toinert carriers. Any conjugation for the sole purpose of increasinghalf-life, rather than to deliver an agent to a target, should beapproached carefully in that Fab′ and other fragments are chosen topenetrate tissues. Nonetheless, conjugation to non-protein polymers,such PEG and the like, is contemplated.

Modifications other than conjugation are therefore based upon modifyingthe structure of the antibody fragment to render it more stable, and/orto reduce the rate of catabolism in the body. One mechanism for suchmodifications is the use of D-amino acids in place of L-amino acids.Those of ordinary skill in the art will understand that the introductionof such modifications needs to be followed by rigorous testing of theresultant molecule to ensure that it still retains the desiredbiological properties. Further stabilizing modifications include the useof the addition of stabilizing moieties to either the N-terminal or theC-terminal, or both, which is generally used to prolong the half-life ofbiological molecules. By way of example only, one may wish to modify thetermini by acylation or amination.

Moderate conjugation-type modifications for use with the presentinvention include incorporating a salvage receptor binding epitope intothe antibody fragment. Techniques for achieving this include mutation ofthe appropriate region of the antibody fragment or incorporating theepitope as a peptide tag that is attached to the antibody fragment. WO96/32478 is specifically incorporated herein by reference for thepurposes of further exemplifying such technology. Salvage receptorbinding epitopes are typically regions of three or more amino acids fromone or two loops of the Fc domain that are transferred to the analogousposition on the antibody fragment. The salvage receptor binding epitopesof WO 98/45331 are incorporated herein by reference for use with thepresent invention.

B12. Binding and Functional Assays

Although the present invention has significant utility in animal andhuman treatment regimens, it also has many other practical uses,including many in vitro uses. Certain of these uses are related to thespecific binding properties of the antibodies or immunoconjugates. Inthat all the compounds of the invention include at least one antibodycomponent, they may be used in virtually all of the binding embodimentsthat the original antibody may be used.

The presence of an attached agent, where relevant, although providingadvantageous properties, does not negate the utility of the firstantibody regions in any binding assay. Suitably useful binding assaysthus include those commonly employed in the art, such as in immunoblots,Western blots, dot blots, RIAs, ELISAs, immunohistochemistry,fluorescent activated cell sorting (FACS), immunoprecipitation, affinitychromatography, and the like, as further described herein.

Certain standard binding assays are those in which an antigen isimmobilized onto a solid support matrix, e.g., nitrocellulose, nylon ora combination thereof, such as in immunoblots, Western blots and relatedassays. Other important assays are ELISAs. All such assays may bereadily adapted for use in the detection of VEGF, as may be applied inthe diagnosis of an angiogenic disease. The agents of the invention mayalso be used in conjunction with both fresh-frozen and formalin-fixed,paraffin-embedded tissue blocks in immunohistochemistry; in fluorescentactivated cell sorting, flow cytometry or flow microfluorometry; inimmunoprecipitation; in antigen purification embodiments, such asaffinity chromatography, even including, in cases of bispecificantibodies, the one-step rapid purification of one or more antigens atthe same time; and in many other binding assays that will be known tothose of skill in the art given the information presented herein.

Further practical uses of the present antibodies are as controls infunctional assays. These include many in vitro and ex vivo assays andsystems, as well as animal model studies. As the binding and functionalproperties of the antibodies of the invention are particularly specific,i.e., they inhibit VEGF binding to and signaling via VEGFR2, but notVEGFR1, such “control” uses are actually extremely valuable. The assaysthat benefit from such a practical application of the present inventioninclude, for example, assays concerning VEGF-mediated endothelial cellgrowth, VEGF-induced phosphorylation and VEGF-induced vascularpermeability, as well as the corneal micropocket assay ofneovascularization and the chick chorio-allantoic membrane assay (CAM)assay. These assays systems can also be developed into in vitro or exvivo drug screening assays, wherein the present provision of biologicalmaterials with well defined properties is particularly important.

C. Immunoconjugates

Although the present invention provides surprisingly effective naked orunconjugated antibodies for use in anti-angiogenic methods,VEGFR2-blocking, anti-VEGF antibody or 2C3-based immunoconjugates,immunotoxins and coaguligands are also provided hereby. Currentlypreferred agents for use in VEGFR2-blocking, anti-VEGF antibody or2C3-based therapeutic conjugates are radiotherapeutic agents (asexemplified by the radiodiagnostics disclosed herein), anti-angiogenicagents, apoptosis-inducing agents, anti-tubulin drugs, anti-cellular orcytotoxic agents and coagulants (coagulation factors).

To generate immunoconjugates, immunotoxins and coaguligands, recombinantexpression may be employed to create a fusion protein, as is known tothose of skill in the art and further disclosed herein. Equally,immunoconjugates, immunotoxins and coaguligands may be generated usingavidin:biotin bridges or any of the chemical conjugation andcross-linker technologies developed in reference to antibody conjugates.

C1. Toxic and Anti-Cellular Agents

For certain applications, the therapeutic agents will be cytotoxic orpharmacological agents, particularly cytotoxic, cytostatic or otherwiseanti-cellular agents having the ability to kill or suppress the growthor cell division of endothelial cells. In general, these aspects of theinvention contemplate the use of any pharmacological agent that can beconjugated to a VEGFR2-blocking, anti-VEGF antibody or 2C3-likeantibody, and delivered in active form to the targeted endothelium.

Exemplary anti-cellular agents include chemotherapeutic agents, as wellas cytotoxins. Chemotherapeutic agents that may be used include:hormones, such as steroids; anti-metabolites, such as cytosinearabinoside, fluorouracil, methotrexate or aminopterin; anthracyclines;mitomycin C; vinca alkaloids; demecolcine; etoposide; mithramycin;anti-tumor alkylating agents, such as chlorambucil or melphalan. Otherembodiments may include agents such as cytokines. Basically, anyanti-cellular agent may be used, so long as it can be successfullyconjugated to, or associated with, an antibody in a manner that willallow its targeting, internalization, release and/or presentation toblood components at the site of the targeted endothelial cells.

There may be circumstances, such as when the target antigen does notinternalize by a route consistent with efficient intoxication by thetoxic compound, where one will desire to target chemotherapeutic agents,such as anti-tumor drugs, cytokines, antimetabolites, alkylating agents,hormones, and the like. A variety of chemotherapeutic and otherpharmacological agents have now been successfully conjugated toantibodies and shown to function pharmacologically, includingdoxorubicin, daunomycin, methotrexate, vinblastine, neocarzinostatin,macromycin, trenimon and ac-amanitin.

In other circumstances, any potential side-effects from cytotoxin-basedtherapy may be eliminated by the use of DNA synthesis inhibitors, suchas daunorubicin, doxorubicin, adriamycin, and the like. These agents aretherefore preferred examples of anti-cellular agents for use in thepresent invention.

In terms of cytostatic agents, such compounds generally disturb thenatural cell cycle of a target cell, preferably so that the cell istaken out of the cell cycle.

A wide variety of cytotoxic agents are known that may be conjugated toVEGFR2-blocking, anti-VEGF antibody or 2C3-based antibodies. Examplesinclude numerous useful plant-, fungus- or bacteria-derived toxins,which, by way of example, include various A chain toxins, particularlyricin A chain; ribosome inactivating proteins, such as saporin orgelonin; α-sarcin; aspergillin; restrictocin; ribonucleases, such asplacental ribonuclease; diphtheria toxin; and pseudomonas exotoxin, toname just a few.

Of the toxins, ricin A chains are preferred. The most preferred toxinmoiety for use herewith is toxin A chain that has been treated to modifyor remove carbohydrate residues, so-called deglycosylated A chain (dgA).Deglycosylated ricin A chain is preferred because of its extremepotency, longer half-life, and because it is economically feasible tomanufacture it in a clinical grade and scale.

It may be desirable from a pharmacological standpoint to employ thesmallest molecule possible that nevertheless provides an appropriatebiological response. One may thus desire to employ smaller A chainpeptides that will provide an adequate anti-cellular response. To thisend, it has been discovered that ricin A chain may be “truncated” by theremoval of 30 N-terminal amino acids by Nagarase (Sigma), and stillretain an adequate toxin activity. It is proposed that where desired,this truncated A chain may be employed in conjugates in accordance withthe invention.

Alternatively, one may find that the application of recombinant DNAtechnology to the toxin A chain moiety will provide additional benefitsin accordance the invention. In that the cloning and expression ofbiologically active ricin A chain has been achieved, it is now possibleto identify and prepare smaller, or otherwise variant peptides, whichnevertheless exhibit an appropriate toxin activity. Moreover, the factthat ricin A chain has now been cloned allows the application ofsite-directed mutagenesis, through which one can readily prepare andscreen for A chain-derived peptides and obtain additional usefulmoieties for use in connection with the present invention.

C2. Coagulation Factors

The VEGFR2-blocking, anti-VEGF antibody or 2C3-based antibodies of theinvention may be linked to a component that is capable of directly orindirectly stimulating coagulation, to form a coaguligand. Here, theantibodies may be directly linked to the coagulant or coagulationfactor, or may be linked to a second binding region that binds and thenreleases the coagulant or coagulation factor. As used herein, the terms“coagulant” and “coagulation factor” are each used to refer to acomponent that is capable of directly or indirectly stimulatingcoagulation under appropriate conditions, preferably when provided to aspecific in vivo environment, such as the tumor vasculature.

Preferred coagulation factors are Tissue Factor compositions, such astruncated TF (tTF), dimeric, multimeric and mutant TF molecules.“Truncated TF” (tTF) refers to TF constructs that are renderedmembrane-binding deficient by removal of sufficient amino acid sequencesto effect this change in property. A “sufficient amount” in this contextis an amount of transmembrane amino acid sequence originally sufficientto enter the TF molecule in the membrane, or otherwise mediatefunctional membrane binding of the TF protein. The removal of such a“sufficient amount of transmembrane spanning sequence” therefore createsa truncated Tissue Factor protein or polypeptide deficient inphospholipid membrane binding capacity, such that the protein issubstantially a soluble protein that does not significantly bind tophospholipid membranes. Truncated TF thus substantially fails to convertFactor VII to Factor VIIa in a standard TF assay, and yet retainsso-called catalytic activity including activating Factor X in thepresence of Factor VIIa.

U.S. Pat. No. 5,504,067 is specifically incorporated herein by referencefor the purposes of further describing such truncated Tissue Factorproteins. Preferably, the Tissue Factors for use in these aspects of thepresent invention will generally lack the transmembrane and cytosolicregions (amino acids 220-263) of the protein. However, there is no needfor the truncated TF molecules to be limited to molecules of the exactlength of 219 amino acids.

Tissue Factor compositions may also be useful as dimers. Any of thetruncated, mutated or other Tissue Factor constructs may be prepared ina dimeric form for use in the present invention. As will be known tothose of ordinary skill in the art, such TF dimers may be prepared byemploying the standard techniques of molecular biology and recombinantexpression, in which two coding regions are prepared in-frame andexpressed from an expression vector. Equally, various chemicalconjugation technologies may be employed in connection with thepreparation of TF dimers. The individual TF monomers may be derivatizedprior to conjugation. All such techniques would be readily known tothose of skill in the art.

If desired, the Tissue Factor dimers or multimers may be joined via abiologically-releasable bond, such as a selectively-cleavable linker oramino acid sequence. For example, peptide linkers that include acleavage site for an enzyme preferentially located or active within atumor environment are contemplated. Exemplary forms of such peptidelinkers are those that are cleaved by urokinase, plasmin, thrombin,Factor IXa, Factor Xa, or a metalloproteinase, such as collagenase,gelatinase or stromelysin.

In certain embodiments, the Tissue Factor dimers may further comprise ahindered hydrophobic membrane insertion moiety, to later encourage thefunctional association of the Tissue Factor with the phospholipidmembrane, but only under certain defined conditions. As described in thecontext of the truncated Tissue Factors, hydrophobicmembrane-association sequences are generally stretches of amino acidsthat promote association with the phospholipid environment due to theirhydrophobic nature. Equally, fatty acids may be used to provide thepotential membrane insertion moiety.

Such membrane insertion sequences may be located either at theN-terminus or the C-terminus of the TF molecule, or generally appendedat any other point of the molecule so long as their attachment theretodoes not hinder the functional properties of the TF construct. Theintent of the hindered insertion moiety is that it remainsnon-functional until the TF construct localizes within the tumorenvironment, and allows the hydrophobic appendage to become accessibleand even further promote physical association with the membrane. Again,it is contemplated that biologically-releasable bonds andselectively-cleavable sequences will be particularly useful in thisregard, with the bond or sequence only being cleaved or otherwisemodified upon localization within the tumor environment and exposure toparticular enzymes or other bioactive molecules.

In other embodiments, the tTF constructs may be multimeric or polymeric.In this context a “polymeric construct” contains 3 or more Tissue Factorconstructs. A “multimeric or polymeric TF construct” is a construct thatcomprises a first TF molecule or derivative operatively attached to atleast a second and a third TF molecule or derivative. The multimers maycomprise between about 3 and about 20 such TF molecules. The individualTF units within the multimers or polymers may also be linked byselectively-cleavable peptide linkers or other biological-releasablebonds as desired. Again, as with the TF dimers discussed above, theconstructs may be readily made using either recombinant manipulation andexpression or using standard synthetic chemistry.

Even further TF constructs useful in context of the present inventionare those mutants deficient in the ability to activate Factor VII. Such“Factor VII activation mutants” are generally defined herein as TFmutants that bind functional Factor VII/VIIa, proteolytically activateFactor X, but are substantially free from the ability to proteolyticallyactivate Factor VII. Accordingly, such constructs are TF mutants thatlack Factor VII activation activity.

The ability of such Factor VII activation mutants to function inpromoting tumor-specific coagulation is based upon their specificdelivery to the tumor vasculature, and the presence of Factor VIIa atlow levels in plasma. Upon administration of such a Factor VIIactivation mutant conjugate, the mutant will be localized within thevasculature of a vascularized tumor. Prior to localization, the TFmutant would be generally unable to promote coagulation in any otherbody sites, on the basis of its inability to convert Factor VII toFactor VIIa. However, upon localization and accumulation within thetumor region, the mutant will then encounter sufficient Factor VIIa fromthe plasma in order to initiate the extrinsic coagulation pathway,leading to tumor-specific thrombosis. Exogenous Factor VIIa could alsobe administered to the patient.

Any one or more of a variety of Factor VII activation mutants may beprepared and used in connection with the present invention. There is asignificant amount of scientific knowledge concerning the recognitionsites on the TF molecule for Factor VII/VIIa. It will thus be understoodthat the Factor VII activation region generally lies between about aminoacid 157 and about amino acid 167 of the TF molecule. However, it iscontemplated that residues outside this region may also prove to berelevant to the Factor VII activating activity, and one may thereforeconsider introducing mutations into any one or more of the residuesgenerally located between about amino acid 106 and about amino acid 209of the TF sequence (WO 94/07515; WO 94/28017; each incorporated hereinby reference).

A variety of other coagulation factors may be used in connection withthe present invention, as exemplified by the agents set forth below.Thrombin, Factor V/a and derivatives, Factor VIII/VIIIa and derivatives,Factor IX/IXa and derivatives, Factor X/Xa and derivatives, FactorXI/XIa and derivatives, Factor XII/XIIa and derivatives, FactorXIII/XIIIa and derivatives, Factor X activator and Factor V activatormay be used in the present invention.

Russell's viper venom Factor X activator is contemplated for use in thisinvention. Monoclonal antibodies specific for the Factor X activatorpresent in Russell's viper venom have also been produced, and could beused to specifically deliver the agent as part of a bispecific bindingligand.

Thromboxane A₂ is formed from endoperoxides by the sequential actions ofthe enzymes cyclooxygenase and thromboxane synthetase in plateletmicrosomes. Thromboxane A₂ is readily generated by platelets and is apotent vasoconstrictor, by virtue of its capacity to produce plateletaggregation. Both thromboxane A₂ and active analogues thereof arecontemplated for use in the present invention.

Thromboxane synthase, and other enzymes that synthesizeplatelet-activating prostaglandins, may also be used as “coagulants” inthe present context. Monoclonal antibodies to, and immunoaffinitypurification of, thromboxane synthase are known; as is the cDNA forhuman thromboxane synthase.

α2-antiplasmin, or α2-plasmin inhibitor, is a proteinase inhibitornaturally present in human plasma that functions to efficiently inhibitthe lysis of fibrin clots induced by plasminogen activator.α2-antiplasmin is a particularly potent inhibitor, and is contemplatedfor use in the present invention.

As the cDNA sequence for α2-antiplasmin is available, recombinantexpression and/or fusion proteins are preferred. Monoclonal antibodiesagainst α2-antiplasmin are also available that may be used in thebispecific binding ligand embodiments of the invention. These antibodiescould both be used to deliver exogenous α2-antiplasmin to the targetsite or to garner endogenous α2-antiplasmin and concentrate it withinthe targeted region.

C3. Anti-Tubulin Drugs

A range of drugs exert their effects via interfering with tubulinactivity. As tubulin functions are essential to mitosis and cellviability, certain “anti-tubulin drugs” are powerful chemotherapeuticagents. Some of the more well known and currently preferred anti-tubulindrugs for use with the present invention are colchicine; taxanes, suchas taxol; vinca alkaloids, such as vinblastine, vincristine andvindescine; and combretastatins. Other suitable anti-tubulin drugs arecytochalasins (including B, J, E), dolastatin, auristatin PE,paclitaxel, ustiloxin D, rhizoxin, 1069C85, colcemid, albendazole,azatoxin and nocodazole.

As described in U.S. Pat. Nos. 5,892,069, 5,504,074 and 5,661,143, eachspecifically incorporated herein by reference, combretastatins areestradiol derivatives that generally inhibit cell mitosis. Exemplarycombretastatins that may be used in conjunction with the inventioninclude those based upon combretastatin A, B and/or D and thosedescribed in U.S. Pat. Nos. 5,892,069, 5,504,074 and 5,661,143.Combretastatins A-1, A-2, A-3, A-4, A-5, A-6, B-1, B-2, B-3 and B-4 areexemplary of the foregoing types.

U.S. Pat. Nos. 5,569,786 and 5,409,953, are incorporated herein byreference for purposes of describing the isolation, structuralcharacterization and synthesis of each of combretastatin A-1, A2, A-3,B-1, B-2, B-3 and B-4 and formulations and methods of using suchcombretastatins to treat neoplastic growth. Any one or more of suchcombretastatins may be used in conjunction with the present invention.

Combretastatin A4, as described in U.S. Pat. Nos. 5,892,069, 5,504,074,5,661,143 and 4,996,237, each specifically incorporated herein byreference, may also be used herewith. U.S. Pat. No. 5,561,122 is furtherincorporated herein by reference for describing suitable combretastatinA-4 prodrugs, which are contemplated for combined use with the presentinvention.

U.S. Pat. No. 4,940,726, specifically incorporated herein by reference,particularly describes macrocyclic lactones denominated combretastatinD-1 and ‘Combretastatin D-2’, each of which may be used in combinationwith the compositions and methods of the present invention. U.S. Pat.No. 5,430,062, specifically incorporated herein by reference, concernsstilbene derivatives and combretastatin analogues with anti-canceractivity that may be used in combination with the present invention.

C4. Anti-Angiogenic Agents

The present invention particularly provides combined anti-angiogenics.The angiopoietins, in common with the members of the VEGF family, aregrowth factors specific for vascular endothelium (Davis and Yancopoulos,1999; Holash et al., 1999; incorporated herein by reference). Theangiopoietins first described were a naturally occurring receptoractivator or agonist, angiopoietin-1 (Ang-1), and a naturally occurringreceptor antagonist, angiopoietin-2 (Ang-2), both of which act by meansof the endothelial cell tyrosine kinase receptor, Tie2.

Two new angiopoietins, angiopoietin-3 (mouse) and angiopoietin4 (human)have also been identified (Valenzuela et al., 1999). Angiopoietin-3appears to act as an antagonist (like Ang-2), whereas angiopoietin-4appears to function as an agonist (like Ang-1) (Valenzuela et al.,1999). A protein termed angiopoietin-3 was also cloned from human heartand reported not to have mitogenic effects on endothelial cells (Kim etal., 1999).

Whereas VEGF is necessary for the early stages of vascular development,angiopoietin-1 is generally required for the later stages ofvascularization. VEGF thus acts to promote endothelial celldifferentiation, proliferation and primitive vessel formation.Angiopoietin-1 acts, via the Tie2 receptor, to promote maintenance andstabilization of mature vessels. Angiopoietin-1 is thus a maturation orstabilization factor, thought to convert immature vessels to immaturevessels by promoting interactions between endothelial cells andsurrounding support cells (Holash et al., 1999).

Angiopoietin-1 has been shown to augment revascularization in ischemictissue (Shyu et al., 1998) and to increase the survival of vascularnetworks exposed to either VEGF or a form of aFGF (Papapetropoulos etal., 1999). These authors also showed that angiopoietin-1 preventsapoptotic death in HUVEC triggered by withdrawal of the same form ofaFGF (Papapetropoulos et al, 1999). Such data are consistent with thedirect role of angiopoietin-1 on human endothelial cells and itsinteraction with other angiogenic molecules to stabilize vascularstructures by promoting the survival of differentiated endothelialcells.

As angiopoietin-1 imparts a maturity and stability signal, the inventorshave carefully conceived those aspects of the present invention thatrelate to targeted angiopoietin-1 delivery. The inventors reasoned thatas angiopoietin-1 is a maturity factor, it will render tumor bloodvessels growth-factor independent. One aspect of this inventiontherefore concerns the use of tumor-targeted angiopoietin-1 in order tocement the VEGF-non-responsive properties of the target vessels.

It is reasoned that using a tumor-binding ligand to deliverangiopoietin-1 to tumor blood vessels would readily deliver on the orderof 500,000 angiopoietin-1 molecules to a vessel lumen. This wouldoverwhelm the Tie2 receptor system, totally saturating the Tie2receptors with the angiopoietin-1 ligand. Angiopoietin-2 would thus beunable to bind, and so the combined effects of angiopoietin-2 and VEGF(see discussion below) would be inhibited.

The delivery of angiopoietin-1 to the tumor, preferably to the tumorvasculature, can also be used in conjunction with a variety of otheranti-cancer strategies, as disclosed in detail herein, to achieve acombined therapeutic effect. The typical response of a tumor totherapies that induce at least some necrosis is to initiate vascularregeneration. As the angiopoietin-1 signal forces the blood vessels intomaturity, they would be unable to remodel and could not compensate forthe loss of tumor mass induced by the primary therapeutic agent. Theseobservations therefore provide another preferred aspect of theangiopoietin delivery invention, namely the combined use ofangiopoietin-1 targeting in combination with any one or more anti-canceragents, including conventional chemotherapeutic drugs.

The action of the angiopoietin-1 upon delivery is fundamentally toprevent vascular remodeling. Whether this is used alone, or incombination therapies, the value of angiopoietin-1 targeting isparticularly enhanced by the safety inherent in this therapeuticapproach. There is no significant downside to angiopoietin-1 therapy.Even in the unlikely event that an amount of the targeted Ang-1 wasmisdirected to non-tumor tissues, all that would result would be thatthe vasculature in the targeted area would become more stable and/orquiescent. In this regard, Ang-1 could also be used as ananti-inflammatory agent.

Angiopoietin-2 is currently a preferred agent for use in tumor-targetedtherapy, particularly in combination with the VEGF inhibition of thepresent invention. However, due to the differential effects ofangiopoietin-2 under different conditions, particularly with varyingVEGF levels, the inventors have again carefully conceived those aspectsof the invention that relate to targeted angiopoietin-2 delivery.

Angiopoietin-2 is also a ligand for the Tie2 receptor, but generallycounteracts blood vessel maturation/stability mediated byangiopoietin-1. It is thus an antagonist of angiopoietin-1 and acts todisturb capillary structure. Under appropriate conditions,angiopoietin-2 imparts a negative signal to the target cells anddestabilization induced by angiopoietin-2 leads to vessel regression.This is the first feature of angiopoietin-2 sought to be exploited inthe targeted delivery of angiopoietin-2 to tumors, preferably to tumorvasculature.

It is contemplated that simply delivering sufficient angiopoietin-2,which is readily achievable using VEGFR2-blocking, anti-VEGF antibodies,such as 2C3, would overwhelm any other signals that could be present inthe tumor environment and would promote vessel regression. As there is acarefully controlled interplay between angiopoietins in the naturalenvironment, an extreme biasing of the system in favor of regression, byperpetual angiopoietin-2 signaling, may well obliterate the effects ofboth angiopoietin-1 and VEGF.

The use of tumor-targeted angiopoietin-2 alone may therefore be used toadvantage to induce tumor vessel regression, particularly as an earlymechanism of therapeutic intervention. Generally, though,destabilization induced by angiopoietin-2 can lead to either vesselregression or regeneration. It is destabilization in the absence ofother angiogenic stimuli, particularly VEGF, which leads to vesselregression; whereas destabilization in the presence of high levels ofVEGF facilitates the angiogenic response (Holash et al., 1999).

Vessels that undergo destabilization in response to angiopoietin-2 canbe “rescued” from regression by exposure to other stimuli.Angiopoietin-2 can therefore render endothelial cells responsive toother angiogenic stimuli and facilitate an angiogenic response underdefined conditions. VEGF, in particular, can prompt ang-2-destabilizedcells to proliferate and form primitive new vessels (Asahara et al.,1998; Holash et al., 1999). Indeed, angiopoietin-2 expression in tumortissue has been reported (Tanaka et al., 1999), where it was presumed toact in combination with VEGF to promote. angiogenesis (Stratmann et al.,1998). The neovascularization initiated by angiopoietin-2 and VEGF makesthese molecules “co-angiogenic”.

A coordinated model to explain the positive and negative effects ofangiopoietin-2 on blood vessels in certain tumor types has now beenreported (Holash et al., 1999). In this model, angiopoietin-2-induceddestabilization initially causes significant vessel regression in tumorsthat originate by coopting blood vessels from surrounding hostvasculature. The high levels of angiopoietin-2 produced bytumor-associated endothelial cells counter the survival signalapparently provided by low-level, constitutive expression ofangiopoietin-1. Angiopoietin-2 thus marks coopted vessels for apoptopicregression (Holash et al., 1999). However, despite the resultant tumornecrosis, surviving tumor cells up-regulate VEGF to ensure theirsurvival. The coincident expression of VEGF and angiopoietin-2 thenresults in robust angiogenesis at the tumor periphery, as VEGF nullifiesthe regressive signal from angiopoietin-2 and in fact promotes vasculardevelopment (Holash et al, 1999).

Although seemingly contradictory on first glance, the actions ofangiopoietin-2 can be explained and largely predicted on the basis ofother signals present, particularly VEGF. In the absence of anotherangiogenic signal, angiopoietin-2 causes vessels to destabilize andbecome immature, leading to regression. In the presence of a stimulus,particularly VEGF, the destabilization caused by angiopoietin-2 actuallyleads to angiogenesis as the vessels are “primed” to receive secondaryangiogenic stimuli. The angiogenic effects of a number of regulators arethus believed to be achieved, at least in part, through the regulationof an autocrine loop of angiopoietin-2 activity in microvascularendothelial cells (Mandriota and Pepper, 1998).

The dual biological roles of angiopoietin-2 prompted the inventors todevelop additional therapeutic strategies that account for other signalsin the tumor environment, particularly VEGF. As angiopoietin-2 and VEGFact in concert to stimulate angiogenesis, a preferred aspect of thepresent invention is to use tumor-targeted angiopoietin-2 delivery incombination with the present VEGF inhibitory antibodies. This willensure that angiopoietin-2 acts in regression and not in angiogenesis.

In light of the foregoing explanations, it will be understood that thepresent invention provides VEGFR2-blocking, anti-VEGF antibodies, suchas 2C3, that are operatively attached to, or otherwise functionallyassociated, with any one or more of angiopoietin-1, angiopoietin-2,angiopoietin-3 and/or angiopoietin-4. Exemplary angiopoietin-1compositions are those of SEQ ID NO:1 (DNA) and SEQ ID NO:2 (protein),whereas angiopoietin-2 compositions are exemplified by SEQ ID NO:3 (DNA)and SEQ ID NO:4 (protein). Angiopoietin-3, being an antagonist, willgenerally be used as angiopoietin-2; and the agonist angiopoietin-4 maybe used in the manner of angiopoietin-1. The article by Valenzuela etal. (1999) is specifically incorporated herein by reference for purposesof further supplementing the present teaching regarding angiopoietin-3and angiopoietin4.

In addition, fusion proteins of angiopoietins are also envisioned foruse in this invention. One example is the stable Ang-1-Ang-2 fusionprotein included herein as SEQ ID NO:5. This protein contains the first73 residues of angiopoietin-2, up to the DAPLEY sequence, fused to theangiopoietin-1 sequence beginning at amino acid 77. It also has amutation at position 265 in the angiopoietin-1 sequence, where Cys isreplaced by Ser.

Other anti-angiogenics for use herewith include angiostatin andendostatin. Angiostatin is disclosed in U.S. Pat. Nos. 5,776,704;5,639,725 and 5,733,876, each incorporated herein by reference.Angiostatin is a protein having a molecular weight of between about 38kD and about 45 kD, as determined by reducing polyacrylamide gelelectrophoresis, which contains approximately Kringle regions 1 through4 of a plasminogen molecule. Angiostatin generally has an amino acidsequence substantially similar to that of a fragment of murineplasminogen beginning at amino acid number 98 of an intact murineplasminogen molecule.

The amino acid sequence of angiostatin varies slightly between species.For example, in human angiostatin, the amino acid sequence issubstantially similar to the sequence of the above described murineplasminogen fragment, although an active human angiostatin sequence maystart at either amino acid number 97 or 99 of an intact humanplasminogen amino acid sequence. Further, human plasminogen may be used,as it has similar anti-angiogenic activity, as shown in a mouse tumormodel.

Angiostatin and endostatin have become the focus of intense study, asthey are the first angiogenesis inhibitors that have demonstrated theability to not only inhibit tumor growth but also cause tumorregressions in nice. There are multiple proteases that have been shownto produce angiostatin from plasminogen including elastase, macrophagemetalloelastase (MME), matrilysin (MMP-7), and 92 kDa gelatinase B/typeIV collagenase (MMP-9).

MME can produce angiostatin from plasminogen in tumors andgranulocyte-macrophage colony-stimulating factor (GMCSF) upregulates theexpression of MME by macrophages inducing the production of angiostatin.The role of MME in angiostatin generation is supported by the findingthat MME is in fact expressed in clinical samples of hepatocellularcarcinomas from patients. Another protease thought to be capable ofproducing angiostatin is stromelysin-1 (MMP-3). MMP-3 has been shown toproduce angiostatin-like fragments from plasminogen in vitro. Themechanism of action for angiostatin is currently unclear, it ishypothesized that it binds to an unidentified cell surface receptor onendothelial cells inducing endothelial cell to undergo programmed celldeath or mitotic arrest.

Endostatin appears to be an even more powerful anti-angiogenesis andanti-tumor agent and is particularly preferred for linking toVEGFR2-blocking, anti-VEGF antibodies, such as 2C3. Endostatin iseffective at causing regressions in a number of tumor models in mice.Tumors do not develop resistance to endostatin and, after multiplecycles of treatment, tumors enter a dormant state during which they donot increase in volume. In this dormant state, the percentage of tumorcells undergoing apoptosis was increased, yielding a population thatessentially stays the same size.

U.S. Pat. No. 5,854,205, to Folkman and O'Reilly, specificallyincorporated herein by reference, concerns endostatin and its use as aninhibitor of endothelial cell proliferation and angiogenesis. Theendostatin protein corresponds to a C-terminal fragment of collagen typeXVIII, and the protein can be isolated from a variety of sources. U.S.Pat. No. 5,854,205 also teaches that endostatin can have an amino acidsequence of a fragment of collagen type XVIII, a collasen type XV, orBOVMPE 1 pregastric esterase. Combinations of endostatin with otheranti-angiogenic proteins, particularly angiostatin, are also describedby U.S. Pat. No. 5,854,205, such that the combined compositions arecapable of effectively regressing the mass of an angiogenesis-dependenttumor.

Endostatin and angiostatin are preferred agents for tumor deliveryaccording to the present invention. Vasculostatin, canstatin and maspinare also preferred agents. Endostatin, in particular, is one of the mostpreferred agents. Endostatin-2C3 fusion proteins may be prepared, asdescribed herein. Various forms of chemically linked endostatin-2C3constructs are also described in the present application.

C5. Apoptosis-Inducing Agents

The present invention may also be used to deliver agents that induceapoptosis in any cells within the tumor, including tumor cells and tumorvascular endothelial cells. Although many anti-cancer agents may have,as part of their mechanism of action, an apoptosis-inducing effect,certain agents have been discovered, designed or selected with this as aprimary mechanism, as described below.

Many forms of cancer have reports of mutations in tumor suppressorgenes, such as p53. Inactivation of p53 results in a failure to promoteapoptosis. With this failure, cancer cells progress in tumorigenesis,rather than become destined for cell death. Thus, delivery of tumorsuppressors is also contemplated for use in the present invention tostimulate cell death. Exemplary tumor suppressors include, but are notlimited to, p53, Retinoblastoma gene (Rb), Wilm's tumor (WT1), baxalpha, interleukin-1b-converting enzyme and family, MEN-1 gene,neurofibromatosis, type 1 (NF1), cdk inhibitor p16, colorectal cancergene (DCC), familial adenomatosis polyposis gene (FAP), multiple tumorsuppressor gene (MTS-1), BRCA1 and BRCA2.

Preferred for use are the p53 (U.S. Pat. Nos. 5,747,469; 5,677,178; and5,756,455; each incorporated herein by reference), Retinoblastoma, BRCA1(U.S. Pat. Nos. 5,750,400; 5,654,155; 5,710,001; 5,756,294; 5,709,999;5,693,473; 5,753,441; 5,622,829; and 5,747,282; each incorporated hereinby reference), MEN-1 (GenBank accession number U93236) and adenovirusEIA (U.S. Pat. No. 5,776,743; incorporated herein by reference) genes.

Other compositions that may be delivered by VEGFR2-blocking, anti-VEGFantibodies, such as 2C3, include genes encoding the tumor necrosisfactor related apoptosis inducing ligand termed TRAIL, and the TRAILpolypeptide (U.S. Pat. No. 5,763,223; incorporated herein by reference);the 24 kD apoptosis-associated protease of U.S. Pat. No. 5,605,826(incorporated herein by reference); Fas-associated factor 1, FAF1 (U.S.Pat. No. 5,750,653; incorporated herein by reference). Also contemplatedfor use in these aspects of the present invention is the provision ofinterleukin-1p-converting enzyme and family members, which are alsoreported to stimulate apoptosis.

Compounds such as carbostyril derivatives (U.S. Pat. Nos. 5,672,603; and5.464,833; each incorporated herein by reference); branched apogenicpeptides (U.S. Pat. No. 5,591,717; incorporated herein by reference);phosphotyrosine inhibitors and non-hydrolyzable phosphotyrosine analogs(U.S. Pat. Nos. 5,565,491; and 5,693,627; each incorporated herein byreference); agonists of RXR retinoid receptors (U.S. Pat. No. 5,399,586;incorporated herein by reference); and even antioxidants (U.S. Pat. No.5,571,523; incorporated herein by reference) may also be used. Tyrosinekinase inhibitors, such as genistein, may also be linked to the agentsof the present invention that target the cell surface receptor, VEGFR1(as supported by U.S. Pat. No. 5,587,459; incorporated herein byreference).

C6. Biologically Functional Equivalents

Equivalents, or even improvements, of 2C3-based antibodies or any otherVEGFR2-blocking, anti-VEGF antibody, can now be made, generally usingthe materials provided above as a starting point. Modifications andchanges may be made in the structure of such an antibody and stillobtain a molecule having like or otherwise desirable characteristics.For example, certain amino acids may substituted for other amino acidsin a protein structure without appreciable loss of interactive bindingcapacity. These considerations also apply to toxins, anti-angiogenicagents, apoptosis-inducing agents, coagulants and the like.

Since it is the interactive capacity and nature of a protein thatdefines that protein's biological functional activity, certain aminoacid sequence substitutions can be made in a protein sequence (or ofcourse, the underlying DNA sequence) and nevertheless obtain a proteinwith like (agonistic) properties. It is thus contemplated that variouschanges may be made in the sequence of the antibodies or therapeuticagents (or underlying DNA sequences) without appreciable loss of theirbiological utility or activity. Biological functional equivalents madefrom mutating an underlying DNA sequence can be made using the codoninformation provided herein in Table A, and the supporting technicaldetails on site-specific mutagenesis.

It also is well understood by the skilled artisan that, inherent in thedefinition of a “biologically functional equivalent” protein or peptide,is the concept that there is a limit to the number of changes that maybe made within a defined portion of the molecule and still result in amolecule with an acceptable level of equivalent biological activity.Biologically functional equivalent proteins and peptides are thusdefined herein as those proteins and peptides in which certain, not mostor all, of the amino acids may be substituted. Of course, a plurality ofdistinct proteins/peptides with different substitutions may easily bemade and used in accordance with the invention.

Amino acid substitutions are generally based on the relative similarityof the amino acid side-chain substituents, for example, theirhydrophobicity, hydrophilicity, charge, size, and the like. An analysisof the size, shape and type of the amino acid side-chain substituentsreveals that arginine, lysine and histidine are all positively chargedresidues; that alanine, glycine and serine are all a similar size; andthat phenylalanine, tryptophan and tyrosine all have a generally similarshape. Therefore, based upon these considerations, arginine, lysine andhistidine; alanine, glycine and serine; and phenylalanine, tryptophanand tyrosine; are defined herein as biologically functional equivalents.

In making more quantitative changes, the hydropathic index of aminoacids may be considered. Each amino acid has been assigned a hydropathicindex on the basis of their hydrophobicity and charge characteristics,these are: isoleucine (+4.5); valine (+4.2); leucine (+3.8);phenylalanine (+2.8); cysteine/cystine (+2.5); methionine (+1.9);alanine (+1.8); glycine (−0.4); threonine (−0.7); serine (−0.8);tryptophan (−0.9); tyrosine (−1.3); proline (−1.6); histidine (−3.2);glutamate (−3.5); glutamine (−3.5); aspartate (−3.5); asparagine (−3.5);lysine (−3.9); and arginine (−4.5).

The importance of the hydropathic amino acid index in conferringinteractive biological function on a protein is generally understood inthe art (Kyte and Doolittle, 1982, incorporated herein by reference). Itis known that certain amino acids may be substituted for other aminoacids having a similar hydropathic index or score and still retain asimilar biological activity. In making changes based upon thehydropathic index, the substitution of amino acids whose hydropathicindices are within ±2 is preferred, those which are within ±1 areparticularly preferred, and those within ±0.5 are even more particularlypreferred.

It is thus understood that an amino acid can be substituted for anotherhaving a similar hydrophilicity value and still obtain a biologicallyequivalent protein. As detailed in U.S. Pat. No. 4,554,101 (incorporatedherein by reference), the following hydrophilicity values have beenassigned to amino acid residues: arginine (+3.0); lysine (+3.0);aspartate (+3.0±1); glutamate (+3.0±1); serine (+0.3); asparagine(+0.2); glutamine (+0.2); glycine (0); threonine (−0.4); proline(−0.5±1); alanine (−0.5); histidine (−0.5); cysteine (−1.0); methionine(−1.3); valine (−1.5); leucine (−1.8); isoleucine (−1.8); tyrosine(−2.3); phenylalanine (−2.5); tryptophan (−3.4).

In making changes based upon hydrophilicity values, the substitution ofamino acids whose hydrophilicity values are within ±2 is preferred,those which are within 1 are particularly preferred, and those within±0.5 are even more particularly preferred.

C7. Fusion Proteins and Recombinant Expression

The VEGFR2-blocking, anti-VEGF antibody or 2C3-based immunoconjugates ofthe present invention may be readily prepared as fusion proteins usingmolecular biological techniques. Any fusion protein may be designed andmade using any of the therapeutic agents disclosed herein and thoseknown in the art. The fusion protein technology is readily adapted toprepare fusion proteins in which the two portions are joined by aselectively cleavable peptide sequence. Currently preferred fusionproteins are those containing endostatin. The endostatin, as with anyother therapeutic, may be attached to the terminus of the antibody or toany point distinct from the CDRs. Therapeutics such as endostatin mayalso be prepared “integrally”, wherein they are preferably associatedwith a selectively cleavable peptide to allow release of the agent aftertargeting.

The use of recombinant DNA techniques to achieve such ends is nowstandard practice to those of skill in the art. These methods include,for example, in vitro recombinant DNA techniques, synthetic techniquesand in vivo recombination/genetic recombination. DNA and RNA synthesismay, additionally, be performed using an automated synthesizers (see,for example, the techniques described in Sambrook et al., 1989;incorporated herein by reference).

The preparation of such a fusion protein generally entails thepreparation of a first and second DNA coding region and the functionalligation or joining of such regions, in frame, to prepare a singlecoding region that encodes the desired fusion protein. In the presentcontext, the VEGFR2-blocking, anti-VEGF antibody or 2C3-like antibodyDNA sequence will be joined in frame with a DNA sequence encoding atherapeutic agent. It is not generally believed to be particularlyrelevant which portion of the construct is prepared as the N-terminalregion or as the C-terminal region.

Once the desired coding region has been produced, an expression vectoris created. Expression vectors contain one or more promoters upstream ofthe inserted DNA regions that act to promote transcription of the DNAand to thus promote expression of the encoded recombinant protein. Thisis the meaning of “recombinant expression”.

To obtain a so-called “recombinant” version of the VEGFR2-blocking,anti-VEGF antibody or 2C3-based immunoconjugate, it is expressed in arecombinant cell. The engineering of DNA segment(s) for expression in aprokaryotic or eukaryotic system may be performed by techniquesgenerally known to those of skill in recombinant expression. It isbelieved that virtually any expression system may be employed in theexpression of a VEGFR2-blocking, anti-VEGF antibody or 2C3-basedimmunoconjugate constructs.

Such proteins may be successfully expressed in eukaryotic expressionsystems, e.g., CHO cells, however, it is envisioned that bacterialexpression systems, such as E. coli pQE-60 will be particularly usefulfor the large-scale preparation and subsequent purification of theVEGFR2-blocking, anti-VEGF antibody or 2C3-based immunoconjugates. cDNAsmay also be expressed in bacterial systems, with the encoded proteinsbeing expressed as fusions with β-galactosidase, ubiquitin, Schistosomajaponicum glutathione S-transferase, and the like. It is believed thatbacterial expression will have advantages over eukaryotic expression interms of ease of use and quantity of materials obtained thereby.

In terms of microbial expression, U.S. Pat. Nos. 5,583,013; 5,221,619;4,785,420; 4,704,362; and 4,366,246 are incorporated herein by referencefor the purposes of even further supplementing the present disclosure inconnection with the expression of genes in recombinant host cells.

Recombinantly produced VEGFR2-blocking, anti-VEGF antibody or 2C3-basedimmunoconjugates may be purified and formulated for humanadministration. Alternatively, nucleic acids encoding theimmunoconjugates may be delivered via gene therapy. Although nakedrecombinant DNA or plasmids may be employed, the use of liposomes orvectors is preferred. The ability of certain viruses to enter cells viareceptor-mediated endocytosis and to integrate into the host cell genomeand express viral genes stably and efficiently have made them attractivecandidates for the transfer of foreign genes into mammalian cells.Preferred gene therapy vectors for use in the present invention willgenerally be viral vectors.

Retroviruses have promise as gene delivery vectors due to their abilityto integrate their genes into the host genome, transferring a largeamount of foreign genetic material, infecting a broad spectrum ofspecies and cell types and of being packaged in special cell-lines.Other viruses, such as adenovirus, herpes simplex viruses (HSV),cytomegalovirus (CMV), and adeno-associated virus (AAV), such as thosedescribed by U.S. Pat. No. 5,139,941 (incorporated herein by reference),may also be engineered to serve as vectors for gene transfer.

Although some viruses that can accept foreign genetic material arelimited in the number of nucleotides they can accommodate and in therange of cells they infect, these viruses have been demonstrated tosuccessfully effect gene expression. However, adenoviruses do notintegrate their genetic material into the host genome and therefore donot require host replication for gene expression, making them ideallysuited for rapid, efficient, heterologous gene expression. Techniquesfor preparing replication-defective infective viruses are well known inthe art.

In certain further embodiments, the gene therapy vector will be HSV. Afactor that makes HSV an attractive vector is the size and organizationof the genome. Because HSV is large, incorporation of multiple genes orexpression cassettes is less problematic than in other smaller viralsystems. In addition, the availability of different viral controlsequences with varying performance (e.g., temporal, strength) makes itpossible to control expression to a greater extent than in othersystems. It also is an advantage that the virus has relatively fewspliced messages, further easing genetic manipulations. HSV also isrelatively easy to manipulate and can be grown to high titers.

Of course, in using viral delivery systems, one will desire to purifythe virion sufficiently to render it essentially free of undesirablecontaminants, such as defective interfering viral particles orendotoxins and other pyrogens such that it will not cause any untowardreactions in the cell, animal or individual receiving the vectorconstruct. A preferred means of purifying the vector involves the use ofbuoyant density gradients, such as cesium chloride gradientcentrifugation.

C8. Antibody Conjugates

VEGFR2-blocking, anti-VEGF antibody or 2C3-based antibodies may beconjugated to anti-cellular or cytotoxic agents, to prepare“immunotoxins”; or operatively associated with components that arecapable of directly or indirectly stimulating coagulation, thus forminga “coaguligand”. In coaguligands, the antibody may be directly linked toa direct or indirect coagulation factor, or may be linked to a secondbinding region that binds and then releases a direct or indirectcoagulation factor. The ‘second binding region’ approach generally usesa coagulant-binding antibody as a second binding region, thus resultingin a bispecific antibody construct. The preparation and use ofbispecific antibodies in general is well known in the art, and isfurther disclosed herein.

In the preparation of immunotoxins, coaguligands and bispecificantibodies, recombinant expression may be employed. The nucleic acidsequences encoding the chosen antibody are attached, in-frame, tonucleic acid sequences encoding the chosen toxin, coagulant, or secondbinding region to create an expression unit or vector. Recombinantexpression results in translation of the new nucleic acid, to yield thedesired protein product. Although antibody-encoding nucleic acids areemployed, rather than protein binding ligands, the recombinant approachis essentially the same as those described hereinabove.

Returning to conjugate technology, the preparation of immunotoxins isgenerally well known in the art. However, certain advantages may beachieved through the application of certain preferred technology, bothin the preparation of the immunotoxins and in their purification forsubsequent clinical administration. For example, while IgG basedimmunotoxins will typically exhibit better binding capability and slowerblood clearance than their Fab′ counterparts, Fab′ fragment-basedimmunotoxins will generally exhibit better tissue penetrating capabilityas compared to IgG based immunotoxins.

Additionally, while numerous types of disulfide-bond containing linkersare known that can be successfully employed to conjugate the toxinmoiety to the VEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody,certain linkers will generally be preferred over other linkers, based ondiffering pharmacological characteristics and capabilities. For example,linkers that contain a disulfide bond that is sterically “hindered” areto be preferred, due to their greater stability in vivo, thus preventingrelease of the toxin moiety prior to binding at the site of action.

A wide variety of cytotoxic agents are known that may be conjugated toVEGFR2-blocking, anti-VEGF antibody or 2C3-based antibodies, includingplant-, fungus- and bacteria-derived toxins, such as ricin A chain ordeglycosylated A chain. The cross-linking of a toxin A chain to anantibody, in certain cases, requires a cross-linker that presentsdisulfide functions. The reason for this is unclear, but is likely dueto a need for certain toxin moieties to be readily releasable from theantibody once the agent has “delivered” the toxin to the targeted cells.

Each type of cross-linker, as well as how the cross-linking isperformed, will tend to vary the pharmacodynamics of the resultantconjugate. Ultimately, in cases where a releasable toxin iscontemplated, one desires to have a conjugate that will remain intactunder conditions found everywhere in the body except the intended siteof action, at which point it is desirable that the conjugate have good“release” characteristics. Therefore, the particular cross-linkingscheme, including in particular the particular cross-linking reagentused and the structures that are cross-linked, will be of somesignificance.

Depending on the specific toxin compound used as part of the fusionprotein, it may be necessary to provide a peptide spacer operativelyattaching the antibody and the toxin compound which is capable offolding into a disulfide-bonded loop structure. Proteolytic cleavagewithin the loop would then yield a heterodimeric polypeptide wherein theantibody and the toxin compound are linked by only a single disulfidebond. An example of such a toxin is a Ricin A-chain toxin.

When certain other toxin compounds are utilized, a non-cleavable peptidespacer may be provided to operatively attach the VEGFR2-blocking,anti-VEGF antibody or 2C3-based antibody and the toxin compound of thefusion protein. Toxins which may be used in conjunction withnon-cleavable peptide spacers are those which may, themselves, beconverted by proteolytic cleavage, into a cytotoxic disulfide-bondedform. An example of such a toxin compound is a Pseudonomas exotoxincompound.

There may be circumstances, such as when the target antigen does notinternalize by a route consistent with efficient intoxication byimmunotoxins, where one will desire to target chemotherapeutic agentssuch as anti-tumor drugs, other cytokines, antimetabolites, alkylatingagents, hormones, and the like. A variety of chemotherapeutic and otherpharmacological agents have now been successfully conjugated toantibodies and shown to function pharmacologically. Exemplaryantineoplastic agents that have been investigated include doxorubicin,daunomycin, methotrexate, vinblastine, and various others. Moreover, theattachment of other agents such as neocarzinostatin, macromycin,trenimon and α-amanitin has been described.

Where coagulation factors are used in connection with the presentinvention, any covalent linkage to the antibody should be made at a sitedistinct from its functional coagulating site. The compositions are thus“linked” in any operative manner that allows each region to perform itsintended function without significant impairment. Thus, the antibodybinds to VEGF, and the coagulation factor promotes blood clotting.

C9. Biochemical Cross-linkers

In additional to the general information provided above,VEGFR2-blocking, anti-VEGF antibody or 2C3-based antibodies may beconjugated to one or more therapeutic agents using certain preferredbiochemical cross-linkers. Cross-linking reagents are used to formmolecular bridges that tie together functional groups of two differentmolecules. To link two different proteins in a step-wise manner,hetero-bifunctional cross-linkers can be used that eliminate unwantedhomopolymer formation. Exemplary hetero-bifunctional cross-linkers arereferenced in Table B1.

TABLE B1 HETERO-BIFUNCTIONAL CROSS-LINKERS Spacer Arm Length LinkerReactive Toward Advantages and Applications after cross-linking SMPTPrimary amines Greater stability 11.2 A Sulfhydryls SPDP Primary aminesThiolation  6.8 A Sulfhydryls Cleavable cross-linking LC-SPDP Primaryamines Extended spacer arm 15.6 A Sulfhydryls Sulfo-LC-SPDP Primaryamines Extended spacer arm 15.6 A Sulfhydryls Water-soluble SMCC Primaryamines Stable maleimide reactive group 11.6 A SulfhydrylsEnzyme-antibody conjugation Hapten-carrier protein conjugationSulfo-SMCC Primary amines Stable maleimide reactive group 11.6 ASulfhydryls Water-soluble Enzyme-antibody conjugation MBS Primary aminesEnzyme-antibody conjugation  9.9 A Sulfhydryls Hapten-carrier proteinconjugation Sulfo-MBS Primary amines Water-soluble  9.9 A SulfhydrylsSIAB Primary amines Enzyme-antibody conjugation 10.6 A SulfhydrylsSulfo-SIAB Primary amines Water-soluble 10.6 A Sulfhydryls SMPB Primaryamines Extended spacer arm 14.5 A Sulfhydryls Enzyme-antibodyconjugation Sulfo-SMPB Primary amines Extended spacer arm 14.5 ASulfhydryls Water-soluble EDC/Sulfo-NHS Primary amines Hapten-Carrierconjugation 0 Carboxyl groups ABH Carbohydrates Reacts with sugar groups11.9 A Nonselective

Hetero-bifunctional cross-linkers contain two reactive groups: onegenerally reacting with primary amine group (e.g., N-hydroxysuccinimide) and the other generally reacting with a thiol group (e.g.,pyridyl disulfide, maleimides, halogens, etc.). Through the primaryamine reactive group, the cross-linker may react with the lysineresidue(s) of one protein (e.g., the selected antibody or fragment) andthrough the thiol reactive group, the cross-linker, already tied up tothe first protein, reacts with the cysteine residue (free sulfhydrylgroup) of the other protein (e.g., the coagulant).

Compositions therefore generally have, or are derivatized to have, afunctional group available for cross-linking purposes. This requirementis not considered to be limiting in that a wide variety of groups can beused in this manner. For example, primary or secondary amine groups,hydrazide or hydrazine groups, carboxyl alcohol, phosphate, oralkylating groups may be used for binding or cross-linking.

The spacer arm between the two reactive groups of a cross-linkers mayhave various length and chemical compositions. A longer spacer armallows a better flexibility of the conjugate components while someparticular components in the bridge (e.g., benzene group) may lend extrastability to the reactive group or an increased resistance of thechemical link to the action of various aspects (e.g., disulfide bondresistant to reducing agents). The use of peptide spacers, such asL-Leu-L-Ala-L-Leu-L-Ala, is also contemplated.

It is preferred that a cross-linker having reasonable stability in bloodwill be employed. Numerous types of disulfide-bond containing linkersare known that can be successfully employed to conjugate targeting andtoxic or coagulating agents. Linkers that contain a disulfide bond thatis sterically hindered may prove to give greater stability in vivo,preventing release of the agent prior to binding at the site of action.These linkers are thus one preferred group of linking agents.

One of the most preferred cross-linking reagents for use in immunotoxinsis SMPT, which is a bifunctional cross-linker containing a disulfidebond that is “sterically hindered” by an adjacent benzene ring andmethyl groups. It is believed that steric hindrance of the disulfidebond serves a function of protecting the bond from attack by thiolateanions such as glutathione which can be present in tissues and blood,and thereby help in preventing. decoupling of the conjugate prior to thedelivery of the attached agent to the tumor site. It is contemplatedthat the SMPT agent may also be used in connection with the bispecificligands of this invention.

The SMPT cross-linking reagent, as with many other known cross-linkingreagents, lends the ability to cross-link functional groups such as theSH of cysteine or primary amines (e.g., the epsilon amino group oflysine). Another possible type of cross-linker includes thehetero-bifunctional photoreactive phenylazides containing a cleavabledisulfide bond such as sulfosuccinimidyl-2-(p-azido salicylamido)ethyl-1,3′-dithiopropionate. The N-hydroxy-succinimidyl group reactswith primary amino groups and the phenylazide (upon photolysis) reactsnon-selectively with any amino acid residue.

In addition to hindered cross-linkers, non-hindered linkers can also beemployed in accordance herewith. Other useful cross-linkers, notconsidered to contain or generate a protected disulfide, include SATA,SPDP and 2-iminothiolane. The use of such cross-linkers is wellunderstood in the art.

Once conjugated, the conjugate is separated from unconjugated targetingand therapeutic agents and from other contaminants. A large a number ofpurification techniques are available for use in providing conjugates ofa sufficient degree of purity to render them clinically useful.Purification methods based upon size separation, such as gel filtration,gel permeation or high performance liquid chromatography, will generallybe of most use. Other chromatographic techniques, such as Blue-Sepharoseseparation, may also be used.

C10. Biologically Releasable Linkers

Although it is preferred that any linking moiety will have reasonablestability in blood, to prevent substantial release of the attached agentbefore targeting to the disease or tumor site, in certain aspects, theuse of biologically-releasable bonds and/or selectively cleavablespacers or linkers is contemplated. “Biologically-releasable bonds” and“selectively cleavable spacers or linkers” still have reasonablestability in the circulation.

The VEGFR2-blocking, anti-VEGF antibodies of the present invention, suchas 2C3-like antibodies, may thus be linked to one or more therapeuticagents via a biologically-releasable bond. Any form of VEGFR2-blocking,anti-VEGF antibody, or “targeting antibody or agent” may be employed,including intact antibodies, although ScFv fragments will be preferredin certain embodiments. “Biologically-releasable bonds” or “selectivelyhydrolyzable bonds” include all linkages that are releasable, cleavableor hydrolyzable only or preferentially under certain conditions. Thisincludes disulfide and trisulfide bonds and acid-labile bonds, asdescribed in U.S. Pat. Nos. 5,474,765 and 5,762,918, each specificallyincorporated herein by reference.

The use of an acid sensitive spacer for attachment of a therapeuticagent or drug to an antibody of the invention is particularlycontemplated. In such embodiments, the therapeutic agents or drugs arereleased within the acidic compartments inside a cell. It iscontemplated that acid-sensitive release may occur extracellularly, butstill after specific targeting, preferably to the tumor site. Certaincurrently preferred examples include 2C3-like antibodies linked tocolchicine or doxorubicin via an acid sensitive spacer. Attachment viathe carbohydrate moieties of the antibodies is also contemplated. Insuch embodiments, the therapeutic agents or drugs are released withinthe acidic compartments inside a cell.

The targeting anti-VEGF antibody may also be derivatized to introducefunctional groups permitting the attachment of the therapeutic agent(s)through a biologically releasable bond. The targeting antibody may thusbe derivatized to introduce side chains terminating in hydrazide,hydrazine, primary amine or secondary amine groups. Therapeutic agentsmay be conjugated through a Schiff's base linkage, a hydrazone or acylhydrazone bond or a hydrazide linker (U.S. Pat. Nos. 5,474,765 and5,762,918, each specifically incorporated herein by reference).

Also as described in U.S. Pat. Nos. 5,474,765 and 5,762,918, eachspecifically incorporated herein by reference, the targeting anti-VEGFantibody may be operatively attached to the therapeutic agent(s) throughone or more biologically releasable bonds that are enzyme-sensitivebonds, including peptide bonds, esters, amides, phosphodiesters andglycosides.

Preferred aspects of the invention concern the use of peptide linkersthat include at least a first cleavage site for a peptidase and/orproteinase that is preferentially located within a disease site,particularly within the tumor environment. The antibody-mediateddelivery of the attached therapeutic agent thus results in cleavagespecifically within the disease site or tumor environment, resulting inthe specific release of the active agent. Certain peptide linkers willinclude a cleavage site that is recognized by one or more enzymesinvolved in remodeling.

Peptide linkers that include a cleavage site for urokinase,pro-urokinase, plasmin, plasminogen, TGFβ, staphylokinase, Thrombin,Factor IXa, Factor Xa or a metalloproteinase, such as an interstitialcollagenase, a gelatinase or a stromelysin, are particularly preferred.U.S. Pat. No. 6,004,555, U.S. Pat. No. 5,877,289, and U.S. applicationSer. No. 08/482,369, Issue Fee paid Oct. 20, 1998, are specificallyincorporated herein by reference for the purpose of further describingand enabling how to make and use targeting agent-therapeutic agentconstructs comprising biologically-releasable bonds andselectively-cleavable linkers and peptides. U.S. Pat. No.5,877,289,issued Mar. 2, 1999, in particular, is specifically incorporated hereinby reference for the purpose of further describing and enabling how tomake and use targeting agent-therapeutic agent constructs that comprisea selectively-cleavable peptide linker that is cleaved by urokinase,plasmin, Thrombin, Factor IXa, Factor Xa or a metalloproteinase, such asan interstitial collagenase, a gelatinase or a stromelysin, within atumor environment.

Currently preferred selectively-cleavable peptide linkers are those thatinclude a cleavage site for plasmin or a metalloproteinase (also knownas “matrix metalloproteases” or “MMPs”), such as an interstitialcollagenase, a gelatinase or a stromelysin. Additional peptide linkersthat may be advantageously used in connection with the present inventioninclude, for example, those listed in Table B2.

TABLE B2 CLEAVABLE LINKER SEQUENCES SEQ Types of Cleavable SequencesAmino Acid Sequence ID NO: Plasmin cleavable sequences Pro-urokinasePRFKIIGG 15 PRFRIIGG 16 TGFβ SSRHRRALD 17 Plasminogen RKSSIIIRMRDVVL 18Staphylokinase SSSFDKGKYKKGDDA 19 SSSFDKGKYKRGDDA 20 Factor Xa cleavablesequences IEGR 21 IDGR 22 GGSIDGR 23 MMP cleavable sequences GelatinaseA PLGLWA 24 Collagenase cleavable sequences Calf skin collagen (α1(I)chain) GPQGIAGQ 25 Calf skin collagen (α2(I) chain) GPQGLLGA 26 Bovinecartilage collagen (α1(II) GIAGQ 27 chain) Human liver collagen (α1(III)chain) GPLGIAGI 28 Human α₂M GPEGLRVG 29 Human PZP YGAGLGVV 30 AGLGVVER31 AGLGISST 32 Rat α₁M EPQALAMS 33 QALAMSAI 34 Rat α₂M AAYHLVSQ 35MDAFLESS 36 Rat α₁I₃(2J) ESLPVVAV 37 Rat α₁I₃(27J) SAPAVESE 38 Humanfibroblast collagenase (autolytic cleavages) DVAQFVLT 39 VAQFVLTE 40AQFVLTEG 41 PVQPIGPQ 42

C11. Bispecific Antibodies

Bispecific antibodies are particularly useful in the coaguligand andcombined anti-angiogenic aspects of the present invention. However,bispecific antibodies in general may be employed, so long as one armbinds to VEGF, optionally at substantially the same epitope as 2C3, andthe bispecific antibody is attached to a therapeutic agent, generally ata site distinct from the antigen binding site.

In general, the preparation of bispecific antibodies is also well knownin the art. One method involves the separate preparation of antibodieshaving specificity for the targeted antigen, on the one hand, and (asherein) a coagulating agent on the other. Peptic F(ab′γ)₂ fragments areprepared from the two chosen antibodies, followed by reduction of eachto provide separate Fab′ySH fragments. The SH groups on one of the twopartners to be coupled are then alkylated with a cross-linking reagentsuch as o-phenylenedimaleimide to provide free maleimide groups on onepartner. This partner may then be conjugated to the other by means of athioether linkage, to give the desired F(ab′γ)₂ heteroconjugate. Othertechniques are known wherein cross-linking with SPDP or protein A iscarried out, or a trispecific construct is prepared.

Another method for producing bispecific antibodies is by the fusion oftwo hybridomas to form a quadroma. As used herein, the term “quadroma”is used to describe the productive fusion of two B cell hybridomas.Using now standard techniques, two antibody producing hybridomas arefused to give daughter cells, and those cells that have maintained theexpression of both sets of clonotype immunoglobulin genes are thenselected.

A preferred method of generating a quadroma involves the selection of anenzyme deficient mutant of at least one of the parental hybridomas. Thisfirst mutant hybridoma cell line is then fused to cells of a secondhybridoma that had been lethally exposed, e.g., to iodoacetamide,precluding its continued survival. Cell fusion allows for the rescue ofthe first hybridoma by acquiring the gene for its enzyme deficiency fromthe lethally treated hybridoma, and the rescue of the second hybridomathrough fusion to the first hybridoma. Preferred, but not required, isthe fusion of immunoglobulins of the same isotype, but of a differentsubclass. A mixed subclass antibody permits the use if an alternativeassay for the isolation of a preferred quadroma.

In more detail, one method of quadroma development and screeninginvolves obtaining a hybridoma line that secretes the first chosen mAband making this deficient for the essential metabolic enzyme,hypoxanthine-guanine phosphoribosyltransferase (HGPRT). To obtaindeficient mutants of the hybridoma, cells are grown in the presence ofincreasing concentrations of 8-azaguanine (1×10⁻⁷M to 1×10⁻⁵M). Themutants are subcloned by limiting dilution and tested for theirhypoxanthine/ aminopterin/ thymidine (HAT) sensitivity. The culturemedium may consist of, for example, DMEM supplemented with 10% FCS, 2 mML-Glutamine and 1 mM penicillin-streptomycin.

A complementary hybridoma cell line that produces the second desired mAbis used to generate the quadromas by standard cell fusion techniques.Briefly, 4.5×10⁷ HAT-sensitive first cells are mixed with 2.8×10⁷HAT-resistant second cells that have been pre-treated with a lethal doseof the irreversible biochemical inhibitor iodoacetamide (5 mM inphosphate buffered saline) for 30 minutes on ice before fusion. Cellfusion is induced using polyethylene glycol (PEG) and the cells areplated out in 96 well microculture plates. Quadromas are selected usingHAT-containing medium. Bispecific antibody-containing cultures areidentified using, for example, a solid phase isotype-specific ELISA andisotype-specific immunofluorescence staining.

In one identification embodiment to identify the bispecific antibody,the wells of microtiter plates (Falcon, Becton Dickinson Labware) arecoated with a reagent that specifically interacts with one of the parenthybridoma antibodies and that lacks cross-reactivity with bothantibodies. The plates are washed, blocked, and the supernatants (SNs)to be tested are added to each well. Plates are incubated at roomtemperature for 2 hours, the supernatants discarded, the plates washed,and diluted alkaline phosphatase-anti-antibody conjugate added for 2hours at room temperature. The plates are washed and a phosphatasesubstrate, e.g., P-Nitrophenyl phosphate (Sigma, St. Louis) is added toeach well. Plates are incubated, 3N NaOH is added to each well to stopthe reaction, and the OD₄₁₀ values determined using an ELISA reader.

In another identification embodiment, microtiter plates pre-treated withpoly-L-lysine are used to bind one of the target cells to each well, thecells are then fixed, e.g. using 1% glutaraldehyde, and the bispecificantibodies are tested for their ability to bind to the intact cell. Inaddition, FACS, immunofluorescence staining, idiotype specificantibodies, antigen binding competition assays, and other methods commonin the art of antibody characterization may be used in conjunction withthe present invention to identify preferred quadromas.

Following the isolation of the quadroma, the bispecific antibodies arepurified away from other cell products. This may be accomplished by avariety of protein isolation procedures, known to those skilled in theart of immunoglobulin purification. Means for preparing andcharacterizing antibodies are well known in the art (See, e.g.,Antibodies: A Laboratory Manual, 1988).

For example, supernatants from selected quadromas are passed overprotein A or protein G sepharose columns to bind IgG (depending on theisotype). The bound antibodies are then eluted with, e.g. a pH 5.0citrate buffer. The elute fractions containing the BsAbs, are dialyzedagainst an isotonic buffer. Alternatively, the eluate is also passedover an anti-immunoglobulin-sepharose column. The BsAb is then elutedwith 3.5 M magnesium chloride. BsAbs purified in this way are thentested for binding activity by, e.g., an isotype-specific ELISA andimmunofluorescence staining assay of the target cells, as describedabove.

Purified BsAbs and parental antibodies may also be characterized andisolated by SDS-PAGE electrophoresis, followed by staining with silveror Coomassie. This is possible when one of the parental antibodies has ahigher molecular weight than the other, wherein the band of the BsAbsmigrates midway between that of the two parental antibodies. Reductionof the samples verifies the presence of heavy chains with two differentapparent molecular weights.

D. Pharmaceutical Compositions

The pharmaceutical compositions of the present invention will generallycomprise an effective amount of at least a first VEGFR2-blocking,anti-VEGF antibody or 2C3-based antibody or immunoconjugate, dissolvedor dispersed in a pharmaceutically acceptable carrier or aqueous medium.Combined therapeutics are also contemplated, and the same type ofunderlying pharmaceutical compositions may be employed for both singleand combined medicaments.

The phrases “pharmaceutically or pharmacologically acceptable” refer tomolecular entities and compositions that do not produce an adverse,allergic or other untoward reaction when administered to an animal, or ahuman, as appropriate. Veterinary uses are equally included within theinvention and “pharmaceutically acceptable” formulations includeformulations for both clinical and/or veterinary use.

As used herein, “pharmaceutically acceptable carrier” includes any andall solvents, dispersion media, coatings, antibacterial and antifungalagents, isotonic and absorption delaying agents and the like. The use ofsuch media and agents for pharmaceutical active substances is well knownin the art. Except insofar as any conventional media or agent isincompatible with the active ingredient, its use in the therapeuticcompositions is contemplated. For human administration, preparationsshould meet sterility, pyrogenicity, general safety and purity standardsas required by FDA Office of Biologics standards. Supplementary activeingredients can also be incorporated into the compositions.

“Unit dosage” formulations are those containing a dose or sub-dose ofthe administered ingredient adapted for a particular timed delivery. Forexample, exemplary “unit dosage“formulations are those containing adaily dose or unit or daily sub-dose or a weekly dose or unit or weeklysub-dose and the like.

D1. Injectable Formulations

The VEGFR2-blocking, anti-VEGF antibody-based and 2C3-based antibodiesor immunoconjugates of the present invention will most often beformulated for parenteral administration, e.g., formulated for injectionvia the intravenous, intramuscular, sub-cutaneous, transdermal, or othersuch routes, including peristaltic administration and directinstillation into a tumor or disease site (intracavity administration).The preparation of an aqueous composition that contains such an antibodyor immunoconjugate as an active ingredient will be known to those ofskill in the art in light of the present disclosure. Typically, suchcompositions can be prepared as injectables, either as liquid solutionsor suspensions; solid forms suitable for using to prepare solutions orsuspensions upon the addition of a liquid prior to injection can also beprepared; and the preparations can also be emulsified.

The pharmaceutical forms suitable for injectable use include sterileaqueous solutions or dispersions; formulations including sesame oil,peanut oil or aqueous propylene glycol; and sterile powders for theextemporaneous preparation of sterile injectable solutions ordispersions. In all cases, the form should be sterile and fluid to theextent that syringability exists. It should be stable under theconditions of manufacture and storage and should be preserved againstthe contaminating action of microorganisms, such as bacteria and fungi.

The VEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody orimmunoconjugate compositions can be formulated into a sterile aqueouscomposition in a neutral or salt form. Solutions as free base orpharmacologically acceptable salts can be prepared in water suitablymixed with a surfactant, such as hydroxypropylcellulose.Pharmaceutically acceptable salts, include the acid addition salts(formed with the free amino groups of the protein), and those that areformed with inorganic acids such as, for example, hydrochloric orphosphoric acids, or such organic acids as acetic, trifluoroacetic,oxalic, tartaric, mandelic, and the like. Salts formed with the freecarboxyl groups can also be derived from inorganic bases such as, forexample, sodium, potassium, ammonium, calcium, or ferric hydroxides, andsuch organic bases as isopropylamine, trimethylamine, histidine,procaine and the like.

Suitable carriers include solvents and dispersion media containing, forexample, water, ethanol, polyol (for example, glycerol, propyleneglycol, and liquid polyethylene glycol, and the like), suitable mixturesthereof, and vegetable oils. In many cases, it will be preferable toinclude isotonic agents, for example, sugars or sodium chloride. Theproper fluidity can be maintained, for example, by the use of a coating,such as lecithin, by the maintenance of the required particle size inthe case of dispersion and/or by the use of surfactants.

Under ordinary conditions of storage and use, all such preparationsshould contain a preservative to prevent the growth of microorganisms.The prevention of the action of microorganisms can be brought about byvarious antibacterial and antifungal agents, for example, parabens,chlorobutanol, phenol, sorbic acid, thimerosal, and the like. Prolongedabsorption of the injectable compositions can be brought about by theuse in the compositions of agents delaying absorption, for example,aluminum monostearate and gelatin.

Prior to or upon formulation, the VEGFR2-blocking, anti-VEGF antibody or2C3-based antibody or immunoconjugate should be extensively dialyzed toremove undesired small molecular weight molecules, and/or lyophilizedfor more ready formulation into a desired vehicle, where appropriate.Sterile injectable solutions are prepared by incorporating the activeagents in the required amount in the appropriate solvent with various ofthe other ingredients enumerated above, as desired, followed by filteredsterilization. Generally, dispersions are prepared by incorporating thevarious sterilized active ingredients into a sterile vehicle thatcontains the basic dispersion medium and the required other ingredientsfrom those enumerated above.

In the case of sterile powders for the preparation of sterile injectablesolutions, the preferred methods of preparation are vacuum-drying andfreeze-drying techniques that yield a powder of the active ingredient,plus any additional desired ingredient from a previouslysterile-filtered solution thereof.

Suitable pharmaceutical compositions in accordance with the inventionwill generally include an amount of the VEGFR2-blocking, anti-VEGFantibody or 2C3-based antibody or immunoconjugate admixed with anacceptable pharmaceutical diluent or excipient, such as a sterileaqueous solution, to give a range of final concentrations, depending onthe intended use. The techniques of preparation are generally well knownin the art as exemplified by Remington's Pharmaceutical Sciences, 16thEd. Mack Publishing Company, 1980, incorporated herein by reference. Itshould be appreciated that endotoxin contamination should be keptminimally at a safe level, for example, less that 0.5 ng/mg protein.Moreover, for human administration, preparations should meet sterility,pyrogenicity, general safety and purity standards as required by FDAOffice of Biological Standards. Upon formulation, the antibody orimmunoconjugate solutions will be administered in a manner compatiblewith the dosage formulation and in such amount as is therapeuticallyeffective.

D2. Sustained Release Formulations

Formulations of VEGFR2-blocking, anti-VEGF antibody-based or 2C3-basedantibodies or immunoconjugate solutions are easily administered in avariety of dosage forms, such as the type of injectable solutionsdescribed above, but other pharmaceutically acceptable forms are alsocontemplated, e.g., tablets, pills, capsules or other solids for oraladministration, suppositories, pessaries, nasal solutions or sprays,aerosols, inhalants, topical formulations, liposomal forms and the like.The type of form for administration will be matched to the disease ordisorder to be treated.

Pharmaceutical “slow release” capsules or “sustained release”compositions or preparations may be used and are generally applicable.Slow release formulations are generally designed to give a constant druglevel over an extended period and may be used to deliver aVEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody orimmunoconjugate in accordance with the present invention. The slowrelease formulations are typically implanted in the vicinity of thedisease site, for example, at the site of a tumor.

Suitable examples of sustained-release preparations includesemipermeable matrices of solid hydrophobic polymers containing theantibody or immunoconjugate, which matrices are in the form of shapedarticles, e.g., films or microcapsule. Examples of sustained-releasematrices include polyesters; hydrogels, for example,poly(2-hydroxyethyl-methacrylate) or poly(vinylalcohol); polylactides,e.g., U.S. Pat. No. 3,773,919; copolymers of L-glutamic acid and γethyl-L-glutamate; non-degradable ethylene-vinyl acetate; degradablelactic acid-glycolic acid copolymers, such as the Lupron Depot™(injectable microspheres composed of lactic acid-glycolic acid copolymerand leuprolide acetate); and poly-D-(−)-3-hydroxybutyric acid.

While polymers such as ethylene-vinyl acetate and lactic acid-glycolicacid enable release of molecules for over 100 days, certain hydrogelsrelease proteins for shorter time periods. When encapsulated antibodiesremain in the body for a long time, they may denature or aggregate as aresult of exposure to moisture at 37° C., thus reducing biologicalactivity and/or changing immunogenicity. Rational strategies areavailable for stabilization depending on the mechanism involved. Forexample, if the aggregation mechanism involves intermolecular S-S bondformation through thio-disulfide interchange, stabilization is achievedby modifying sulfhydryl residues, lyophilizing from acidic solutions,controlling moisture content, using appropriate additives, developingspecific polymer matrix compositions, and the like.

D3. Liposomes and Nanoparticles

In certain embodiments, liposomes and/or nanoparticles may also beemployed with the VEGFR2-blocking, anti-VEGF antibody or 2C3-basedantibodies or immunoconjugates. The formation and use of liposomes isgenerally known to those of skill in the art, as summarized below.

Liposomes are formed from phospholipids that are dispersed in an aqueousmedium and spontaneously form multilamellar concentric bilayer vesicles(also termed multilamellar vesicles (MLVs). MLVs generally havediameters of from 25 nm to 4 μm. Sonication of MLVs results in theformation of small unilamellar vesicles (SUVs) with diameters in therange of 200 to 500 Å, containing an aqueous solution in the core.

Phospholipids can form a variety of structures other than liposomes whendispersed in water, depending on the molar ratio of lipid to water. Atlow ratios, the liposome is the preferred structure. The physicalcharacteristics of liposomes depend on pH, ionic strength and thepresence of divalent cations. Liposomes can show low permeability toionic and polar substances, but at elevated temperatures undergo a phasetransition which markedly alters their permeability. The phasetransition involves a change from a closely packed, ordered structure,known as the gel state, to a loosely packed, less-ordered structure,known as the fluid state. This occurs at a characteristicphase-transition temperature and results in an increase in permeabilityto ions, sugars and drugs.

Liposomes interact with cells via four different mechanisms: Endocytosisby phagocytic cells of the reticuloendothelial system such asmacrophages and neutrophils; adsorption to the cell surface, either bynonspecific weak hydrophobic or electrostatic forces, or by specificinteractions with cell-surface components; fusion with the plasma cellmembrane by insertion of the lipid bilayer of the liposome into theplasma membrane, with simultaneous release of liposomal contents intothe cytoplasm; and by transfer of liposomal lipids to cellular orsubcellular membranes, or vice versa, without any association of theliposome contents. Varying the liposome formulation can alter whichmechanism is operative, although more than one may operate at the sametime.

Nanocapsules can generally entrap compounds in a stable and reproducibleway. To avoid side effects due to intracellular polymeric overloading,such ultrafine particles (sized around 0.1 μm) should be designed usingpolymers able to be degraded in vivo. Biodegradablepolyalkyl-cyanoacrylate nanoparticles that meet these requirements arecontemplated for use in the present invention, and such particles may beare easily made.

D4. Ophthalmic Formulations

Many diseases with an angiogenic component are associated with the eye.For example, diseases associated with corneal neovascularization thatcan be treated according to the present invention include, but are notlimited to, diabetic retinopathy, retinopathy of prematurity, cornealgraft rejection, neovascular glaucoma and retrolental fibroplasia,epidemic keratoconjunctivitis, Vitamin A deficiency, contact lensoverwear, atopic keratitis, superior limbic keratitis, pterygiumkeratitis sicca, sjogrens, acne rosacea, phylectenulosis, syphilis,Mycobacteria infections, lipid degeneration, chemical burns, bacterialulcers, fungal ulcers, Herpes simplex infections, Herpes zosterinfections, protozoan infections, Kaposi sarcoma, Mooren ulcer,Terrien's marginal degeneration, mariginal keratolysis, trauma,rheumatoid arthritis, systemic lupus, polyarteritis, Wegenerssarcoidosis, Scleritis, Steven's Johnson disease, periphigoid radialkeratotomy, and corneal graph rejection.

Diseases associated with retinal/choroidal neovascularization that canbe treated according to the present invention include, but are notlimited to, diabetic retinopathy, macular degeneration, sickle cellanemia, sarcoid, syphilis, pseudoxanthoma elasticum, Pagets disease,vein occlusion, artery occlusion, carotid obstructive disease, chronicuveitis/vitritis, mycobacterial infections, Lyme's disease, systemiclupus erythematosis, retinopathy of prematurity, Eales disease, Bechetsdisease, infections causing a retinitis or choroiditis, presumed ocularhistoplasmosis, Bests disease, myopia, optic pits, Stargarts disease,pars planitis, chronic retinal detachment, hyperviscosity syndromes,toxoplasmosis, trauma and post-laser complications.

Other diseases that can be treated according to the present inventioninclude, but are not limited to, diseases associated with rubeosis(neovascularization of the angle) and diseases caused by the abnormalproliferation of fibrovascular or fibrous tissue including all forms ofproliferative vitreoretinopathy, whether or not associated withdiabetes.

The VEGFR2-blocking, anti-VEGF antibody-based and 2C3-based antibodiesand immunoconjugates of the present invention may thus be advantageouslyemployed in the preparation of pharmaceutical compositions suitable foruse as ophthalmic solutions, including those for intravitreal and/orintracameral administration. For the treatment of any of the foregoingor other disorders a VEGFR2-blocking, anti-VEGF antibody or 2C3-basedantibody composition of the invention would be administered to the eyeor eyes of the subject in need of treatment in the form of an ophthalmicpreparation prepared in accordance with conventional pharmaceuticalpractice, see for example “Remington's Pharmaceutical Sciences” 15thEdition, pages 1488 to 1501 (Mack Publishing Co., Easton, Pa.).

The ophthalmic preparation will contain a VEGFR2-blocking, anti-VEGFantibody or 2C3-based antibody in a concentration from about 0.01 toabout 1% by weight, preferably from about 0.05 to about 0.5% in apharmaceutically acceptable solution, suspension or ointment. Somevariation in concentration will necessarily occur, depending on theparticular compound employed, the condition of the subject to be treatedand the like, and the person responsible for treatment will determinethe most suitable concentration for the individual subject. Theophthalmic preparation will preferably be in the form of a sterileaqueous solution containing, if desired, additional ingredients, forexample preservatives, buffers, tonicity agents, antioxidants andstabilizers, nonionic wetting or clarifying agents, viscosity-increasingagents and the like.

Suitable preservatives for use in such a solution include benzalkoniumchloride, benzethonium chloride, chlorobutanol, thimerosal and the like.Suitable buffers include boric acid, sodium and potassium bicarbonate,sodium and potassium borates, sodium and potassium carbonate, sodiumacetate, sodium biphosphate and the like, in amounts sufficient tomaintain the pH at between about pH 6 and pH 8, and preferably, betweenabout pH 7 and pH 7.5. Suitable tonicity agents are dextran 40, dextran70, dextrose, glycerin, potassium chloride, propylene glycol, sodiumchloride, and the like, such that the sodium chloride equivalent of theophthalmic solution is in the range 0.9 plus or minus 0.2%.

Suitable antioxidants and stabilizers include sodium bisulfite, sodiummetabisulfite, sodium thiosulfite, thiourea and the like. Suitablewetting and clarifying agents include polysorbate 80, polysorbate 20,poloxamer 282 and tyloxapol. Suitable viscosity-increasing agentsinclude dextran 40, dextran 70, gelatin, glycerin,hydroxyethylcellulose, hydroxmethylpropylcellulose, lanolin,methylcellulose, petrolatum, polyethylene glycol, polyvinyl alcohol,polyvinylpyrrolidone, carboxymethylcellulose and the like. Theophthalmic preparation will be administered topically to the eye of thesubject in need of treatment by conventional methods, for example in theform of drops or by bathing the eye in the ophthalmic solution.

D5. Topical Formulations

In the broadest sense, formulations for topical administration includethose for delivery via the mouth (buccal) and through the skin. “Topicaldelivery systems” also include transdermal patches containing theingredient to be administered. Delivery through the skin can further beachieved by iontophoresis or electrotransport, if desired.

Formulations suitable for topical administration in the mouth includelozenges comprising the ingredients in a flavored basis, usually sucroseand acacia or tragacanth; pastilles comprising the active ingredient inan inert basis such as gelatin and glycerin, or sucrose and acacia; andmouthwashes comprising the ingredient to be administered in a suitableliquid carrier.

Formulations suitable for topical administration to the skin includeointments, creams, gels and pastes comprising the ingredient to beadministered in a pharmaceutical acceptable carrier. The formulation ofVEGFR2-blocking, anti-VEGF or 2C3-based antibodies for topical use, suchas in creams, ointments and gels, includes the preparation of oleaginousor water-soluble ointment bases, as is well known to those in the art.For example, these compositions may include vegetable oils, animal fats,and more preferably, semisolid hydrocarbons obtained from petroleum.Particular components used may include white ointment, yellow ointment,cetyl esters wax, oleic acid, olive oil, paraffin, petrolatum, whitepetrolatum, spermaceti, starch glycerite, white wax, yellow wax,lanolin, anhydrous lanolin and glyceryl monostearate. Variouswater-soluble ointment bases may also be used, including glycol ethersand derivatives, polyethylene glycols, polyoxyl 40 stearate andpolysorbates.

Formulations for rectal administration may be presented as a suppositorywith a suitable base comprising, for example, cocoa butter or asalicylate. Formulations suitable for vaginal administration may bepresented as pessaries, tampons, creams, gels, pastes, foams or sprayformulations containing in addition to the active ingredient suchcarriers as are known in the art to be appropriate.

D6. Nasal Formulations

Local delivery via the nasal and respiratory routes is contemplated fortreating various conditions. These delivery routes are also suitable fordelivering agents into the systemic circulation. Formulations of activeingredients in carriers suitable for nasal administration are thereforealso included within the invention, for example, nasal solutions,sprays, aerosols and inhalants. Where the carrier is a solid, theformulations include a coarse powder having a particle size, forexample, in the range of 20 to 500 microns, which is administered, e.g.,by rapid inhalation through the nasal passage from a container of thepowder held close up to the nose.

Suitable formulations wherein the carrier is a liquid are useful innasal administration. Nasal solutions are usually aqueous solutionsdesigned to be administered to the nasal passages in drops or sprays andare prepared so that they are similar in many respects to nasalsecretions, so that normal ciliary action is maintained. Thus, theaqueous nasal solutions usually are isotonic and slightly buffered tomaintain a pH of 5.5 to 6.5. In addition, antimicrobial preservatives,similar to those used in ophthalmic preparations, and appropriate drugstabilizers, if required, may be included in the formulation. Variouscommercial nasal preparations are known and include, for example,antibiotics and antihistamines and are used for asthma prophylaxis.

Inhalations and inhalants are pharmaceutical preparations designed fordelivering a drug or compound into the respiratory tree of a patient. Avapor or mist is administered and reaches the affected area. This routecan also be employed to deliver agents into the systemic circulation.Inhalations may be administered by the nasal or oral respiratory routes.The administration of inhalation solutions is only effective if thedroplets are sufficiently fine and uniform in size so that the mistreaches the bronchioles.

Another group of products, also known as inhalations, and sometimescalled insufflations, comprises finely powdered or liquid drugs that arecarried into the respiratory passages by the use of special deliverysystems, such as pharmaceutical aerosols, that hold a solution orsuspension of the drug in a liquefied gas propellant. When releasedthrough a suitable valve and oral adapter, a metered does of theinhalation is propelled into the respiratory tract of the patient.Particle size is of major importance in the administration of this typeof preparation. It has been reported that the optimum particle size forpenetration into the pulmonary cavity is of the order of 0.5 to 7 μm.Fine mists are produced by pressurized aerosols and hence their use inconsidered advantageous.

E. Therapeutic Kits

This invention also provides therapeutic kits comprising aVEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody orimmunoconjugate for use in the present treatment methods. Such kits willgenerally contain, in suitable container means, a pharmaceuticallyacceptable formulation of at least one VEGFR2-blocking, anti-VEGFantibody or 2C3-based antibody or immunoconjugate. The kits may alsocontain other pharmaceutically acceptable formulations, either fordiagnosis/imaging or combined therapy. For example, such kits maycontain any one or more of a range of chemotherapeutic orradiotherapeutic drugs; anti-angiogenic agents; anti-tumor cellantibodies; and/or anti-tumor vasculature or anti-tumor stromaimmunotoxins or coaguligands.

The kits may have a single container (container means) that contains theVEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody orimmunoconjugate, with or without any additional components, or they mayhave distinct containers for each desired agent. Where combinedtherapeutics are provided, a single solution may be pre-mixed, either ina molar equivalent combination, or with one component in excess of theother. Alternatively, each of the VEGFR2-blocking, anti-VEGF antibody or2C3-based antibody or immunoconjugate and other anti-cancer agentcomponents of the kit may be maintained separately within distinctcontainers prior to administration to a patient.

When the components of the kit are provided in one or more liquidsolutions, the liquid solution is preferably an aqueous solution, with asterile aqueous solution being particularly preferred. However, thecomponents of the kit may be provided as dried powder(s). When reagentsor components are provided as a dry powder, the powder can bereconstituted by the addition of a suitable solvent. It is envisionedthat the solvent may also be provided in another container.

The containers of the kit will generally include at least one vial, testtube, flask, bottle, syringe or other container means, into which theVEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody orimnmunoconjugate, and any other desired agent, may be placed and,preferably, suitably aliquoted. Where separate components are included,the kit will also generally contain a second vial or other containerinto which these are placed, enabling the administration of separateddesigned doses. The kits may also comprise a second/third containermeans for containing a sterile, pharmaceutically acceptable buffer orother diluent.

The kits may also contain a means by which to administer theVEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody orimmunoconjugate to an animal or patient, e.g., one or more needles orsyringes, or even an eye dropper, pipette, or other such like apparatus,from which the formulation may be injected into the animal or applied toa diseased area of the body. The kits of the present invention will alsotypically include a means for containing the vials, or such like, andother component, in close confinement for commercial sale, such as,e.g., injection or blow-molded plastic containers into which the desiredvials and other apparatus are placed and retained.

F. Anti-Angiogenic Therapy

The present invention may be used to treat animals and patients withaberrant angiogenesis, such as that contributing to a variety ofdiseases and disorders. The most prevalent and/or clinically importantof these, outside the field of cancer treatment, include arthritis,rheumatoid arthritis, psoriasis, atherosclerosis, diabetic retinopathy,age-related macular degeneration, Grave's disease, vascular restenosis,including restenosis following angioplasty, arteriovenous malformations(AVM), meningioma, hemangioma and neovascular glaucoma. Other potentialtargets for intervention include angiofibroma, atherosclerotic plaques,corneal graft neovascularization, hemophilic joints, hypertrophic scars,osler-weber syndrome, pyogenic granuloma retrolental fibroplasia,scleroderma, trachoma, vascular adhesions, synovitis, dermatitis,various other inflammatory diseases and disorders, and evenendometriosis. Further diseases and disorders that are treatable by theinvention, and the unifying basis of such angiogenic disorders, are setforth below.

One disease in which angiogenesis is involved is rheumatoid arthritis,wherein the blood vessels in the synovial lining of the joints undergoangiogenesis. In addition to forming new vascular networks, theendothelial cells release factors and reactive oxygen species that leadto pannus growth and cartilage destruction. The factors involved inangiogenesis may actively contribute to, and help maintain, thechronically inflamed state of rheumatoid arthritis. Factors associatedwith angiogenesis also have a role in osteoarthritis, contributing tothe destruction of the joint.

Harada et al. (1998, specifically incorporated herein by reference)showed that VEGF is involved in the pathogenesis of rheumatoid arthritisand, furthermore, that measurement of serum concentration of VEGF is anoninvasive, useful method for monitoring the disease activity ofrheumatoid arthritis. This supports the therapeutic and diagnostic usesof the present invention in connection with rheumatoid arthritis.

Nagashima et al. (1999, specifically incorporated herein by reference)described the inhibitory effects of anti-rheumatic drugs on VEGF incultured rheumatoid synovial cells. VEGF is constitutively expressed inthe synovium of rheumatoid arthritis. The known anti-rheumatic drug,bucillamine (BUC), was shown to include within its mechanism of actionthe inhibition of VEGF production by synovial cells. Thus, theanti-rheumatic effects of BUC are mediated by suppression ofangiogenesis and synovial proliferation in the arthritic synoviumthrough the inhibition of VEGF production by synovial cells. The use ofthe present invention as an anti-arthritic therapy is supported by theVEGF inhibitory actions of this existing therapeutic.

Another example of a disease mediated by angiogenesis is ocularneovascular disease. This disease is characterized by invasion of newblood vessels into the structures of the eye, such as the retina orcornea. It is the most common cause of blindness and is involved inapproximately twenty eye diseases. In age-related macular degeneration,the associated visual problems are caused by an ingrowth of chorioidalcapillaries through defects in Bruch's membrane with proliferation offibrovascular tissue beneath the retinal pigment epithelium. Angiogenicdamage is also associated with diabetic retinopathy, retinopathy ofprematurity, corneal graft rejection, neovascular glaucoma andretrolental fibroplasia.

Other diseases associated with corneal neovascularization include, butare not limited to, epidemic keratoconjunctivitis, Vitamin A deficiency,contact lens overwear, atopic keratitis, superior limbic keratitis,pterygium keratitis sicca, sjogrens, acne rosacea, phylectenulosis,syphilis, Mycobacteria infections, lipid degeneration, chemical bums,bacterial ulcers, fungal ulcers, Herpes simplex infections, Herpeszoster infections, protozoan infections, Kaposi sarcoma, Mooren ulcer,Terrien's marginal degeneration, mariginal keratolysis, rheumatoidarthritis, systemic lupus, polyarteritis, trauma, Wegeners sarcoidosis,Scleritis, Steven's Johnson disease, periphigoid radial keratotomy, andcorneal graph rejection.

Diseases associated with retinal/choroidal neovascularization include,but are not limited to, diabetic retinopathy, macular degeneration,sickle cell anemia, sarcoid, syphilis, pseudoxanthoma elasticum, Pagetsdisease, vein occlusion, artery occlusion, carotid obstructive disease,chronic uveitis/vitritis, mycobacterial infections, Lyme's disease,systemic lupus erythematosis, retinopathy of prematurity, Eales disease,Bechets disease, infections causing a retinitis or choroiditis, presumedocular histoplasmosis, Bests disease, myopia, optic pits, Stargartsdisease, pars planitis, chronic retinal detachment, hyperviscositysyndromes, toxoplasmosis, trauma and post-laser complications.

Other diseases include, but are not limited to, diseases associated withrubeosis (neovascularization of the angle) and diseases caused by theabnormal proliferation of fibrovascular or fibrous tissue including allforms of proliferative vitreoretinopathy.

Chronic inflammation also involves pathological angiogenesis. Suchdisease states as ulcerative colitis and Crohn's disease showhistological changes with the ingrowth of new blood vessels into theinflamed tissues. Bartonellosis, a bacterial infection found in SouthAmerica, can result in a chronic stage that is characterized byproliferation of vascular endothelial cells.

Another pathological role associated with angiogenesis is found inatherosclerosis. The plaques formed within the lumen of blood vesselshave been shown to have angiogenic stipulatory activity. VEGF expressionin human coronary atherosclerotic lesions was demonstrated by Inoue etal. (1998, specifically incorporated herein by reference). Thisevidences the pathophysiological significance of VEGF in the progressionof human coronary atherosclerosis, as well as in recanalizationprocesses in obstructive coronary diseases. The present inventionprovides an effective treatment for such conditions.

One of the most frequent angiogenic diseases of childhood is thehemangioma. In most cases, the tumors are benign and regress withoutintervention. In more severe cases, the tumors progress to largecavernous and infiltrative forms and create clinical complications.Systemic forms of hemangiomas, the hemangiomatoses, have a highmortality rate. Therapy-resistant hemangiomas exist that cannot betreated with therapeutics currently in use.

Angiogenesis is also responsible for damage found in hereditary diseasessuch as Osler-Weber-Rendu disease, or hereditary hemorrhagictelangiectasia. This is an inherited disease characterized by multiplesmall angiomas, tumors of blood or lymph vessels. The angiomas are foundin the skin and mucous membranes, often accompanied by epistaxis(nosebleeds) or gastrointestinal bleeding and sometimes with pulmonaryor hepatic arteriovenous fistula.

Angiogenesis is also involved in normal physiological processes such asreproduction and wound healing. Angiogenesis is an important step inovulation and also in implantation of the blastula after fertilization.Prevention of angiogenesis could be used to induce amenorrhea, to blockovulation or to prevent implantation by the blastula.

In wound healing, excessive repair or fibroplasia can be a detrimentalside effect of surgical procedures and may be caused or exacerbated byangiogenesis. Adhesions are a frequent complication of surgery and leadto problems such as small bowel obstruction.

Diseases and disorders characterized by undesirable vascularpermeability can also be treated by the present invention. These includeedema associated with brain tumors, ascites associated withmalignancies, Meigs' syndrome, lung inflammation, nephrotic syndrome,pericardial effusion and pleural effusion, as disclosed in WO 98/16551,specifically incorporated herein by reference.

Each of the foregoing diseases and disorders, along with all types oftumors, as described in the following sections, can be effectivelytreated by the present invention in accordance with the knowledge in theart, as disclosed in, e.g., U.S. Pat. No. 5,712,291 (specificallyincorporated herein by reference), that unified benefits result from theapplication of anti-angiogenic strategies to the treatment of angiogenicdiseases.

The antibodies and/or immunoconjugates of the invention are mostpreferably utilized in the treatment of tumors. Tumors in whichangiogenesis is important include malignant tumors, and benign tumors,such as acoustic neuroma, neurofibroma, trachoma and pyogenicgranulomas. Angiogenesis is particularly prominent in solid tumorformation and metastasis. However, angiogenesis is also associated withblood-born tumors, such as leukemias, and various acute or chronicneoplastic diseases of the bone marrow in which unrestrainedproliferation of white blood cells occurs, usually accompanied byanemia, impaired blood clotting, and enlargement of the lymph nodes,liver, and spleen. Angiogenesis also plays a role in the abnormalitiesin the bone marrow that give rise to leukemia-like tumors.

Angiogenesis is important in two stages of tumor metastasis. In thevascularization of the primary tumor, angiogenesis allows cells to enterthe blood stream and to circulate throughout the body. After tumor cellshave left the primary site, and have settled into the secondary,metastasis site, angiogenesis must occur before the new tumor can growand expand. Therefore, prevention of angiogenesis can prevent metastasisof tumors and contain the neoplastic growth at the primary site,allowing treatment by other therapeutics, particularly, therapeuticagent-targeting agent constructs (see below).

The VEGFR2-blocking, anti-VEGF antibody and 2C3-based antibody orimmunoconjugate methods provided by this invention are thus broadlyapplicable to the treatment of any malignant tumor having a vascularcomponent. In using the antibodies and/or immunoconjugates of theinvention in the treatment of tumors, particularly vascularized,malignant tumors, the agents may be used alone or in combination with,e.g., chemotherapeutic, radiotherapeutic, apoptopic, anti-angiogenicagents and/or immunotoxins or coaguligands.

Typical vascularized tumors for treatment are the solid tumors,particularly carcinomas, which require a vascular component for theprovision of oxygen and nutrients. Exemplary solid tumors that may betreated using the invention include, but are not limited to, carcinomasof the lung, breast, ovary, stomach, pancreas, larynx, esophagus,testes, liver, parotid, biliary tract, colon, rectum, cervix, uterus,endometrium, kidney, bladder, prostate, thyroid, squamous cellcarcinomas, adenocarcinomas, small cell carcinomas, melanomas, gliomas,glioblastomas, neuroblastomas, and the like. WO 98/45331 is alsoincorporated herein by reference to further exemplify the variety oftumor types that may be effectively treated using an anti-VEGF antibody.

Knowledge of the role of angiogenesis in the maintenance and metastasisof tumors has led to a prognostic indicator for cancers such as breastcancer. The amount of neovascularization found in the primary tumor wasdetermined by counting the microvessel density in the area of the mostintense neovascularization in invasive breast carcinoma. A high level ofmicrovessel density was found to correlate with tumor recurrence.Control of angiogenesis by the therapies of the present invention willreduce or negate the recurrence of such tumors.

The present invention is contemplated for use in the treatment of anypatient that presents with a solid tumor. In light of the specificproperties of the VEGFR2-blocking, anti-VEGF antibody-basedcompositions, the therapeutics of the present invention will havereduced side effects. Particular advantages will result in themaintenance or enhancement of host immune responses against the tumor,as mediated by macrophages, and in the lack of adverse effects on bonetissue. The invention will thus be the anti-angiogenic therapy of choicefor the treatment of pediatric cancers and patients having, or at riskfor developing, osteoporosis and other bone deficiencies.

Although all malignancies and solid tumors may be treated by theinvention, the unconjugated VEGFR2-blocking, anti-VEGF and 2C3antibodies of this invention are particularly contemplated for use intreating patients with more angiogenic tumors, or patients at risk formetastasis.

The present invention is also intended as a preventative or prophylactictreatment. These aspects of the invention include the ability of theinvention to treat patients presenting with a primary tumor who may havemetastatic tumors, or tumor cells in the earlier stages of metastatictumor seeding. As an anti-angiogenic strategy, the present invention mayalso be used to prevent tumor development in subjects at moderate orhigh risk for developing a tumor, as based upon prognostic tests and/orclose relatives suffering from a hereditary cancer.

The conjugated or immunotoxin forms of the VEGFR2-blocking, anti-VEGFand 2C3 antibodies of the invention are particularly contemplated foruse in destroying or de-bulking solid tumors. These aspects of theinvention may be used in conjunction with the unconjugatedanti-angiogenic antibodies of the invention, or with otheranti-angiogenic approaches.

It will be readily appreciated by those of skill in the art that theimmunoconjugate and prodrug forms of the present treatment methods havethe distinct advantage of providing a single therapeutic agent with twoproperties: the inherent anti-angiogenic property of the antibody andthe therapeutic property of the attached agent (e.g., cytotoxic,coagulative, apoptopic, etc). The conjugated and prodrug treatment formsof the present antibodies thus have an incredibly wide utilitythroughout the field of cancer treatment.

The guidance provided herein regarding the more suitable patients foruse in connection with the different aspects of the present invention isintended as teaching that certain patient's profiles may assist with theselection of patients for treatment by the present invention. Thepre-selection of certain patients, or categories of patients, does notin any way negate the usefulness of the present invention in connectionwith the treatment of all patients having a vascularized tumor, or otherangiogenic disease as described above. A further consideration is thefact that the assault on the tumor provided by the invention maypredispose the tumor to further therapeutic treatment, such that thesubsequent treatment results in an overall synergistic effect or evenleads to total remission or cure.

It is not believed that any particular type of tumor should be excludedfrom treatment using the present invention. However, the type of tumorcells may be relevant to the use of the invention in combination withother therapeutic agents, particularly chemotherapeutics and anti-tumorcell immunotoxins. Both the unconjugated and conjugated aspects of thepresent therapies will include an anti-angiogenic effect that willinhibit tumor vasculature proliferation. The conjugated and prodrugtreatment aspects will further destroy or occlude the tumor vasculature.As the vasculature is substantially or entirely the same in all solidtumors, the present methodology will be understood to be widely orentirely applicable to the treatment of all solid tumors, irrespectiveof the particular phenotype or genotype of the tumor cells themselves.

Therapeutically effective doses of VEGFR2-blocking, anti-VEGF antibodiesor 2C3-based antibody or immunoconjugate constructs are readilydeterminable using data from an animal model, e.g., as shown in thestudies detailed herein. Experimental animals bearing solid tumors arefrequently used to optimize appropriate therapeutic doses prior totranslating to a clinical environment. Such models are known to be veryreliable in predicting effective anti-cancer strategies. For example,mice bearing solid tumors, such as used in the Examples, are widely usedin pre-clinical testing. The inventors have used such art-accepted mousemodels to determine working ranges of therapeutic agents that givebeneficial anti-tumor effects with minimal toxicity.

In using unconjugated VEGFR2-blocking, anti-VEGF antibodies or 2C3-basedantibodies in anti-angiogenic therapies, one can also draw on otherpublished data in order to assist in the formulation of doses forclinical treatment. For instance, although the antibodies of the presentinvention have distinct advantages over those in the art, theinformation in the literature concerning treatment with other anti-VEGFantibodies can still be used in combination with the data and teachingin the present application to design and/or optimize treatment protocolsand doses.

For example, Borgstrom et al. (1999), specifically incorporated hereinby reference, described the importance of VEGF in breast cancerangiogenesis in vivo using MAb A4.6.1. As the 2C3-like antibodies ofthis invention exhibited equivalent or even improved anti-tumorresponses in comparative studies with A4.6.1, these antibodies will alsohave significant utility in the treatment of breast cancer. Theinventors further realized, as will be appreciated by those of ordinaryskill in the art, that patients with breast cancer are typically womenin the middle or later age groups, where concerns regarding osteoporosisare also apparent. The VEGFR2-blocking, anti-VEGF antibody and 2C3-basedantibodies of the present invention will thus have the added advantageof not causing an adverse effect on bone metabolism, and so will not bepreferred for use in breast cancer patients having or at risk fordeveloping osteoporosis.

The same type of benefits make VEGFR2-blocking, anti-VEGF antibody and2C3-based therapeutics the preferred drugs for the treatment ofpediatric cancers. In children with cancer, the need to continue healthyand substantial bone growth is evident. As VEGFR2-blocking, anti-VEGFantibodies, such as 2C3, will not substantially impair the activities ofosteoclasts and chondroclasts, which are important in developing bone,2C3 will have important advantages over other antibodies, such asA4.6.1.

Borgstrom et al. (1999), specifically incorporated herein by reference,also reported that MAb A4.6.1 resulted in significant tumors regressionwhen used in combination with doxorubicin. This further supports thecombined use of VEGFR2-blocking, anti-VEGF antibodies and conventionalcytotoxic or chemotherapeutic agents to achieve significant clinicalresults in treating a variety of cancers. Both unconjugated doxorubicinand doxorubicin prodrug combinations are contemplated.

Ferrara and colleagues also reported on the efficacy andconcentration-response of a murine anti-VEGF monoclonal antibody intumor-bearing mice and the extrapolation to human treatment (Mordenti etal., 1999, specifically incorporated herein by reference). The studieswere designed to evaluate the concentration-response relationship of themurine anti-VEGF monoclonal antibody so that an efficacious plasmaconcentration of the recombinant humanized form of the antibody could beestimated in cancer patients. Mordenti et al. (1999) concluded thatsatisfactory tumor suppression in nude mice was achieved using doses ofthe murine antibody that could be readily applied to the human system inorder to define clinical dosing regimens effective to maintain atherapeutic antibody for human use in the required efficacious range.Accordingly, the data from the present art-accepted mouse models canalso be translated into appropriate human doses using the type ofanalyses reported in Mordenti et al. (1999), in addition to thetechniques known to the skilled artisan as described herein.

Results from preclinical safety evaluations of a recombinant, humanizedform of Genentech's anti-VEGF antibody in monkeys (Ryan et al., 1999,specifically incorporated herein by reference) serve to exemplify thedrawbacks with that particular candidate therapeutic. Although theantibody has pharmacological activity in this animal, the monkeys inthese studies exhibited physeal dysplasia characterized by adose-related increase in hypertrophied chondrocytes, subchondral bonyplate formation, and inhibition of vascular invasion of the growthplate. No such drawbacks will be evident in the use of theVEGFR2-blocking, anti-VEGF antibody and 2C3-based therapeutics, which donot inhibit VEGF

Data from a further study on the preclinical pharmacokinetics,interspecies scaling and tissue distribution of Genentech's humanizedmonoclonal anti-VEGF antibody was reported by Lin et al. (1999,specifically incorporated herein by reference). These studies wereconducted in mice, rats, monkeys and rabbits, the latter using¹²⁵I-labelled antibody. The pharmacokinetic data from mice, rats andmonkeys were used to predict the pharmacokinetics of the humanizedcounterpart antibody using allometric scaling in humans. Accordingly,appropriate dosage information can be developed for the treatment ofhuman pathological conditions, such as rheumatoid arthritis, ocularneovascularization and cancer.

A humanized version of the anti-VEGF antibody A4.6.1 has been employedin clinical trials as an anti-cancer agent (Brem, 1998; Baca et al.,1997; Presta et al., 1997; each incorporated herein by reference).Therefore, such clinical data can also be considered as a referencesource when designing therapeutic doses for the present VEGFR2-blocking,anti-VEGF antibody and 2C3 treatment. The present invention shows 2C3 tobe as effective as A4.6.1 in studies in tumor-bearing mice, although thespecificity for inhibiting only VEGFR2-mediated actions of VEGF is anadvantage. WO 98/45331 is also incorporated herein by reference tofurther exemplify the doses of humanized anti-VEGF antibodies that maybe used in treatment.

In terms of using conjugated VEGFR2-blocking, anti-VEGF antibodies or2C3-based immunoconjugates in tumor therapy, one may refer to thescientific and patent literature on the success of delivering a widerange of therapeutics to tumor vasculature to achieve a beneficialeffect. By way of example, each of U.S. Pat. Nos. 5,855,866; 5,877,289;5,965,132; 6,051,230; 6,004,555; 5,776,427; 6,004,554; and 6,036,955;and U.S. Ser. No. 08/482,369, Issue Fee paid Oct. 20, 1998 areincorporated herein by reference for the purpose of further describingthe use of such therapeutic agent-targeting agent constructs. In thepresent case, the therapeutic agent-targeting agent constructs includetargeting agent portions that exert an anti-angiogenic effect, whichwill magnify or otherwise enhance the anti-tumor activity of theattached therapeutic agent.

As is known in the art, there are realistic objectives that may be usedas a guideline in connection with pre-clinical testing before proceedingto clinical treatment. However, in light of the progress of otheranti-VEGF antibodies to the clinic, the demonstrated anti-tumor effectsin accepted models shown herein, and the enhanced safety of the presentstrategies, the current invention provides a therapeutic with a fasttrack to clinical treatment. Thus, pre-clinical testing may be employedto select the most advantageous antibodies, doses or combinations.

Any VEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody orimmunoconjugate dose, or combined medicament, that results in anyconsistently detectable anti-angiogenic effect, inhibition ofmetastasis, tumor vasculature destruction, tumor thrombosis, necrosisand/or general anti-tumor effect will define a useful invention. Thepresent invention may also be effective against vessels downstream ofthe tumor, .e., target at least a sub-set of the draining vessels,particularly as cytokines released from the tumor will be acting onthese vessels, changing their antigenic profile.

It will also be understood that even in such circumstances where theanti-angiogenic and/or tumor effects of the VEGFR2-blocking, anti-VEGFantibody or 2C3-based antibody or immunoconjugate dose, or combinedtherapy, are towards the low end of the intended therapeutic range, itmay be that this therapy is still equally or even more effective thanall other known therapies in the context of the particular tumor targetor patient. It is unfortunately evident to a clinician that certaintumors and conditions cannot be effectively treated in the intermediateor long term, but that does not negate the usefulness of the presenttherapy, particularly where it is at least about as effective as theother strategies generally proposed.

In designing appropriate doses of VEGFR2-blocking, anti-VEGF antibody or2C3-based antibody or immunoconjugate constructs, or combinedtherapeutics, for the treatment of vascularized tumors, one may readilyextrapolate from the animal studies described herein and the knowledgein the literature in order to arrive at appropriate doses for clinicaladministration. To achieve a conversion from animal to human doses, onewould account for the mass of the agents administered per unit mass ofthe experimental animal and, preferably, account for the differences inthe body surface area (m²) between the experimental animal and the humanpatient. All such calculations are well known and routine to those ofordinary skill in the art.

For example, taking the successful doses of 2C3 in the mouse studies,and by applying standard calculations based upon mass and surface area,effective doses for use in human patients would be between about 1 mg/m²and about 1000 mg/m², preferably, between about 50 mg/r² and 500mg/m²10, and most preferably, between about 10 mg/m² and about 100mg/m². These doses are appropriate for VEGFR2-blocking, anti-VEGFantibody or 2C3-based naked antibodies and VEGFR2-blocking, anti-VEGFantibody or 2C3-based immunoconjugates, although the doses are preferredfor use in connection with naked or unconjugated antibodies for use asanti-angiogenics.

Accordingly, using this information, the inventors contemplate thatuseful low doses of VEGFR2-blocking, anti-VEGF antibody or 2C3-basedantibodies or immunoconjugates for human administration will be about 1,2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 15, 20, 25, 30, 35, 40, 45 or about 50mg/m²; and that useful high doses of such antibodies or immunoconjugatesfor human administration will be about 600, 650, 700, 750, 800, 850,900, 925, 950, 975 or about 1000 mg/m². Useful intermediate doses ofVEGFR2-blocking, anti-VEGF antibody or 2C3-based antibodies orimmunoconjugates for human administration are contemplated to be anydose between the low and high ranges, such as about 55, 60, 70, 80, 90,100, 125, 150, 175, 200, 250, 300, 350, 400, 450, 500, 525, 550 or about575 mg/M² or so.

Any particular range using any of the foregoing recited exemplary dosesor any value intermediate between the particular stated ranges iscontemplated. Where VEGFR2-blocking, anti-VEGF antibody or 2C3-basedimmunoconjugates are used, it will also be understood that coagulantimmunoconjugates can generally be used at higher doses than toxinimmunoconjugates.

In general, dosage ranges of between about 10-100 mg/m², about 10-90mg/m², about 10-80 mg/m², about 20-100 mg/m², about 20-90 mg/m², about20-80 mg/m², about 30-100 mg/m², about 30-90 mg/m², about 30-80 mg/m²,about 15-100 mg/m², about 25-100 mg/m², about 35-100mg/m², about 15-90mg/m², about 25-90 mg/m², about 35-90 mg/m², or so of VEGFR2-blocking,anti-VEGF antibody or 2C3-based antibodies or immunoconjugates will bepreferred. Notwithstanding these stated ranges, it will be understoodthat, given the parameters and detailed guidance presented herein,further variations in the active or optimal ranges will be encompassedwithin the present invention.

Therefore, it will be understood that lower doses may be moreappropriate in combination with other agents, and that high doses canstill be tolerated, particularly given the enhanced safety of theVEGFR2-blocking, anti-VEGF antibody and 2C3-based antibodies that bindonly to VEGFR2 and the yet further enhanced safety of VEGFR2-blocking,anti-VEGF antibody and 2C3-based coagulant and anti-angiogenicimmunoconjugates. The use of human or humanized antibodies (andoptionally, human coagulant or anti-angiogenic proteins) renders thepresent invention even safer for clinical use, further reducing thechances of significant toxicity or side effects in healthy tissues.

The intention of the therapeutic regimens of the present invention isgenerally to produce significant anti-tumor effects whilst still keepingthe dose below the levels associated with unacceptable toxicity. Inaddition to varying the dose itself, the administration regimen can alsobe adapted to optimize the treatment strategy. One treatment protocol isto administer between about 1 mg/m² and about 1000 mg/m², preferably,between about 50 mg/m² and 500 mg/m²10, and most preferably, betweenabout 10 mg/m² and about 100 mg/m² of the VEGFR2-blocking, anti-VEGFantibody or 2C3-based antibody or immunoconjugate, or therapeuticcocktail containing such, about 1 to 3 times a week, preferably byintravenous or intramuscular administration, and most preferably,intravenously.

In administering the particular doses, one would preferably provide apharmaceutically acceptable composition (according to FDA standards ofsterility, pyrogenicity, purity and general safety) to the patientsystemically. Intravenous injection is generally preferred. Continuousinfusion over a time period of about 1 or 2 hours or so is alsocontemplated.

Naturally, before wide-spread use, clinical trials will be conducted.The various elements of conducting a clinical trial, including patienttreatment and monitoring, will be known to those of skill in the art inlight of the present disclosure. The following information is beingpresented as a general guideline for use in establishing such trials.

Patients chosen for the first VEGFR2-blocking, anti-VEGF antibody or2C3-based treatment studies will have failed to respond to at least onecourse of conventional therapy, and will have objectively measurabledisease as determined by physical examination, laboratory techniques,and/or radiographic procedures. Any chemotherapy should be stopped atleast 2 weeks before entry into the study. Where murine monoclonalantibodies or antibody portions are employed, the patients should haveno history of allergy to mouse immunoglobulin.

Certain advantages will be found in the use of an indwelling centralvenous catheter with a triple lumen port. The VEGFR2-blocking, anti-VEGFantibody or 2C3-based agents should be filtered, for example, using a0.22μ filter, and diluted appropriately, such as with saline, to a finalvolume of 100 ml. Before use, the test sample should also be filtered ina similar manner, and its concentration assessed before and afterfiltration by determining the A₂₈₀. The expected recovery should bewithin the range of 87% to 99%, and adjustments for protein loss canthen be accounted for.

The VEGFR2-blocking, anti-VEGF antibody or 2C3-based antibodies orconjugates may be administered over a period of approximately 4-24hours, with each patient receiving 2-4 infusions at 2-7 day intervals.Administration can also be performed by a steady rate of infusion over a7 day period. The infusion given at any dose level should be dependentupon any toxicity observed. Hence, if Grade II toxicity was reachedafter any single infusion, or at a particular period of time for asteady rate infusion, further doses should be withheld or the steadyrate infusion stopped unless toxicity improved. Increasing doses ofVEGFR2-blocking, anti-VEGF antibody or 2C3-based therapeutics should beadministered to groups of patients until approximately 60% of patientsshowed unacceptable Grade III or IV toxicity in any category. Doses thatare 2/3 of this value are defined as the safe dose.

Physical examination, tumor measurements, and laboratory tests should,of course, be performed before treatment and at intervals up to 1 monthlater. Laboratory tests should include complete blood counts, serumcreatinine, creatine kinase, electrolytes, urea, nitrogen, SGOT,bilirubin, albumin, and total serum protein. Serum samples taken up to60 days after treatment should be evaluated by radioimmunoassay for thepresence of the administered therapeutic, and antibodies against anyportions thereof. Immunological analyses of sera, using any standardassay such as, for example, an ELISA or RIA, will allow thepharmacokinetics and clearance of the VEGFR2-blocking, anti-VEGFantibody or 2C3-based therapeutic agent to be evaluated.

To evaluate the anti-tumor responses, the patients should be examined at48 hours to 1 week and again at 30 days after the last infusion. Whenpalpable disease was present, two perpendicular diameters of all massesshould be measured daily during treatment, within 1 week aftercompletion of therapy, and at 30 days. To measure nonpalpable disease,serial CT scans could be performed at 1-cm intervals throughout thechest, abdomen, and pelvis at 48 hours to 1 week and again at 30 days.Tissue samples should also be evaluated histologically, and/or by flowcytometry, using biopsies from the disease sites or even blood or fluidsamples if appropriate.

Clinical responses may be defined by acceptable measure. For example, acomplete response may be defined by the disappearance of all measurabletumor 1 month after treatment. Whereas a partial response may be definedby a 50% or greater reduction of the sum of the products ofperpendicular diameters of all evaluable tumor nodules 1 month aftertreatment, with no tumor sites showing enlargement. Similarly, a mixedresponse may be defined by a reduction of the product of perpendiculardiameters of all measurable lesions by 50% or greater 1 month aftertreatment, with progression in one or more sites.

In light of results from clinical trials, such as those described above,an even more precise treatment regimen may be formulated. Even so, somevariation in dosage may later be necessary depending on the condition ofthe subject being treated. The physician responsible for administrationwill, in light of the present disclosure, be able to determine theappropriate dose for the individual subject. Such optimization andadjustment is routinely carried out in the art and by no means reflectsan undue amount of experimentation.

G. Combination Therapies

Whether used for treating angiogenic diseases, such as arthritis,psoriasis, atherosclerosis, diabetic retinopathy, age-related maculardegeneration, Grave's disease, vascular restenosis, hemangioma andneovascular glaucoma (or other diseases described above), or solidtumors, the present invention can be combined with other therapies.

The VEGFR2-blocking, anti-VEGF antibody or 2C3-based treatment methodsof the present invention may be combined with any other methodsgenerally employed in the treatment of the particular tumor, disease ordisorder that the patient exhibits. So long as a particular therapeuticapproach is not known to be detrimental to the patient's condition initself, and does not significantly counteract the VEGFR2-blocking,anti-VEGF antibody or 2C3-based treatment, its combination with thepresent invention is contemplated.

In connection solid tumor treatment, the present invention may be usedin combination with classical approaches, such as surgery, radiotherapy,chemotherapy, and the like. The invention therefore provides combinedtherapies in which VEGFR2-blocking, anti-VEGF antibody or 2C3-basedconstructs are used simultaneously with, before, or after surgery orradiation treatment; or are administered to patients with, before, orafter conventional chemotherapeutic, radiotherapeutic or anti-angiogenicagents, or targeted immunotoxins or coaguligands.

The combined use of the invention with radiotherapy, radiotherapeutics,anti-angiogenic agents, apoptosis-inducing agents and anti-tubulin drugsis particularly preferred. Many examples of such agents have beendescribed above in conjunction with the immunoconjugates of the presentinvention. Any of the agents initially described for use as one part ofa therapeutic conjugate may also be used separately, but still inoperable combination with the present invention.

When one or more agents are used in combination with theVEGFR2-blocking, anti-VEGF antibody or 2C3-based therapy, there is norequirement for the combined results to be additive of the effectsobserved when each treatment is conducted separately. Although at leastadditive effects are generally desirable, any increased anti-tumoreffect above one of the single therapies would be of benefit. Also,there is no particular requirement for the combined treatment to exhibitsynergistic effects, although this is certainly possible andadvantageous.

To practice combined anti-tumor therapy, one would simply administer toan animal a VEGFR2-blocking, anti-VEGF antibody or 2C3-based constructin combination with another anti-cancer agent in a manner effective toresult in their combined anti-tumor actions within the animal. Theagents would therefore be provided in amounts effective and for periodsof time effective to result in their combined presence within the tumorvasculature and their combined actions in the tumor environment. Toachieve this goal, the VEGFR2-blocking, anti-VEGF antibody or 2C3-basedtherapeutic and anti-cancer agents may be administered to the animalsimultaneously, either in a single composition, or as two distinctcompositions using different administration routes.

Alternatively, the VEGFR2-blocking, anti-VEGF antibody or 2C3-basedtreatment may precede, or follow, the anti-cancer agent treatment by,e.g., intervals ranging from minutes to weeks and months. One wouldensure that the anti-cancer agent and VEGFR2-blocking, anti-VEGFantibody or 2C3-based agent exert an advantageously combined effect onthe tumor.

Most anti-cancer agents would be given prior to VEGFR2-blocking,anti-VEGF antibody or 2C3-based anti-angiogenic therapy. However, whereVEGFR2-blocking, anti-VEGF antibody or 2C3-based immunoconjugates areused, various anti-cancer agents may be simultaneously or subsequentlyadministered.

The general use of combinations of substances in cancer treatment iswell know. For example, U.S. Pat. No. 5,710,134 (incorporated herein byreference) discloses components that induce necrosis in tumors incombination with non-toxic substances or “prodrugs”. The enzymes setfree by necrotic processes cleave the non-toxic “prodrug” into the toxic“drug”, which leads to tumor cell death. Also, U.S. Pat. No. 5,747,469(incorporated herein by reference) discloses the combined use of viralvectors encoding p53 and DNA damaging agents. Any such similarapproaches can be used with the present invention.

In some situations, it may even be desirable to extend the time periodfor treatment significantly, where several days (2, 3, 4, 5, 6 or 7),several weeks (1, 2, 3, 4, 5, 6, 7 or 8) or even several months (1, 2,3, 4, 5, 6, 7 or 8) lapse between the respective administrations. Thiswould be advantageous in circumstances where one treatment was intendedto substantially destroy the tumor, such as surgery or chemotherapy, andanother treatment was intended to prevent micrometastasis or tumorre-growth, such as anti-angiogenic based therapy. Anti-angiogenicsshould be administered at a careful time after surgery to alloweffective wound healing.

It also is envisioned that more than one administration of either theVEGFR2-blocking, anti-VEGF antibody or 2C3-based agent or theanti-cancer agent will be utilized. The agents may be administeredinterchangeably, on alternate days or weeks; or a sequence ofVEGFR2-blocking, anti-VEGF antibody or 2C3-based treatment may be given,followed by a sequence of anti-cancer agent therapy. In any event, toachieve tumor regression using a combined therapy, all that is requiredis to deliver both agents in a combined amount effective to exert ananti-tumor effect, irrespective of the times for administration.

In terms of surgery, any surgical intervention may be practiced incombination with the present invention. In connection with radiotherapy,any mechanism for inducing DNA damage locally within tumor cells iscontemplated, such as γ-irradiation, X-rays, UV-irradiation, microwavesand even electronic emissions and the like. The directed delivery ofradioisotopes to tumor cells is also contemplated, and this may be usedin connection with a targeting antibody or other targeting means, andpreferably, VEGFR2-blocking, anti-VEGF antibodies, such as 2C3.

Cytokine therapy also has proven to be an effective partner for combinedtherapeutic regimens. Various cytokines may be employed in such combinedapproaches. Examples of cytokines include IL-1α IL-1β, IL-2, IL-3, IL-4,IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12, IL-13, TGF-β, GM-CSF,M-CSF, G-CSF, TNFα, TNFβ, LAF, TCGF, BCGF, TRF, BAF, BDG, MP, LIF, OSM,TMF, PDGF, IFN-α, IFN-β, IFN-γ. Cytokines are administered according tostandard regimens, consistent with clinical indications such as thecondition of the patient and relative toxicity of the cytokine.Uteroglobins may also be used to prevent or inhibit metastases (U.S.Pat. No. 5,696,092; incorporated herein by reference).

G1. Chemotherapeutics

In certain embodiments, the VEGFR2-blocking, anti-VEGF antibody or2C3-based therapeutic agents of the present invention may beadministered in combination with a chemotherapeutic agent. A variety ofchemotherapeutic agents may be used in the combined treatment methodsdisclosed herein. Chemotherapeutic agents contemplated as exemplaryinclude, e.g., adriamycin, dactinomycin, mitomycin, carminomycin,daunomycin, doxorubicin, tamoxifen, taxol, taxotere, vincristine,vinblastine, vinorelbine, etoposide (VP-16), 5-fluorouracil (5FU),cytosine arabinoside, cyclophohphamide, thiotepa, methotrexate,camptothecin, actinomycin-D, mitomycin C, cisplatin (CDDP), aminopterin,combretastatin(s) and derivatives and prodrugs thereof.

As will be understood by those of ordinary skill in the art, theappropriate doses of chemotherapeutic agents will be generally aroundthose already employed in clinical therapies wherein thechemotherapeutics are administered alone or in combination with otherchemotherapeutics. By way of example only, agents such as cisplatin, andother DNA alkylating may be used. Cisplatin has been widely used totreat cancer, with efficacious doses used in clinical applications of 20mg/m² for 5 days every three weeks for a total of three courses.Cisplatin is not absorbed orally and must therefore be delivered viainjection intravenously, subcutaneously, intratumorally orintraperitoneally.

Further useful agents include compounds that interfere with DNAreplication, mitosis and chromosomal segregation. Such chemotherapeuticcompounds include adriamycin, also known as doxorubicin, etoposide,verapamil, podophyllotoxin, and the like. Widely used in a clinicalsetting for the treatment of neoplasms, these compounds are administeredthrough bolus injections intravenously at doses ranging from 25-75 mg/m²at 21 day intervals for adriamycin, to 35-50 mg/m² for etoposideintravenously or double the intravenous dose orally.

Agents that disrupt the synthesis and fidelity of polynucleotideprecursors may also be used. Particularly useful are agents that haveundergone extensive testing and are readily available. As such, agentssuch as 5-fluorouracil (5-FU) are preferentially used by neoplastictissue, making this agent particularly useful for targeting toneoplastic cells. Although quite toxic, 5-FU, is applicable in a widerange of carriers, including topical, however intravenous administrationwith doses ranging from 3 to 15 mg/kg/day being commonly used.

Exemplary chemotherapeutic agents for combined therapy are listed inTable C. Each of the agents listed are exemplary and not limiting. Theskilled artisan is directed to “Remington's Pharmaceutical Sciences”15th Edition, chapter 33, in particular pages 624-652. Variation indosage will likely occur depending on the condition being treated. Thephysician administering treatment will be able to determine theappropriate dose for the individual subject.

TABLE C CHEMOTHERAPEUTIC AGENTS USEFUL IN NEOPLASTIC DISEASENONPROPRIETARY NAMES CLASS TYPE OF AGENT (OTHER NAMES) DISEASEAlkylating Nitrogen Mustards Mechlorethamine (HN₂) Hodgkin's disease,non-Hodgkin's Agents lymphomas Cyclophosphamide Acute and chroniclymphocytic ifosfamide leukemias, Hodgkin's disease, non- Hodgkin'slymphomas, multiple myeloma, neuroblastoma, breast, ovary, lung, Wilms'tumor, cervix, testis, soft-tissue sarcomas Melphalan (L-sarcolysin)Multiple myeloma, breast, ovary Chlorambucil Chronic lymphocyticleukemia, primary macroglobulinemia, Hodgkin's disease, non-Hodgkin'slymphomas Ethylenimenes and Hexamethylmelamine Ovary MethylmelaminesThiotepa Bladder, breast, ovary Alkyl Sulfonates Busulfan Chronicgranulocytic leukemia Nitrosoureas Carmustine (BCNU) Hodgkin's disease,non-Hodgkin's lymphomas, primary brain tumors, multiple myeloma,malignant melanoma Lomustine (CCNU) Hodgkin's disease, non-Hodgkin'slymphomas, primary brain tumors, small-cell lung Semustine (methyl-CCNU)Primary brain tumors, stomach, colon Streptozocin Malignant pancreaticinsulinoma, (streptozotocin) malignant carcinoid Triazines Dacarbazine(DTIC; Malignant melanoma, Hodgkin's dimethyltriazenoimidaz disease,soft-tissue sarcomas olecarboxamide) Antimetabolites Folic Acid AnalogsMethotrexate Acute lymphocytic leukemia, (amethopterin) choriocarcinoma,mycosis fungoides, breast, head and neck, lung, osteogenic sarcomaPyrimidine Analogs Fluoracil (5-fluorouracil; Breast, colon, stomach,pancreas, 5-FU) ovary, head and neck, urinary bladder, Floxuridine(fluorode- premalignant skin lesions (topical) oxyuridine; FUdR)Cytarabine (cytosine Acute granulocytic and acute arabinoside)lymphocytic leukemias Mercaptopurine Acute lymphocytic, acute(6-mercaptopurine; granulocytic and chronic granulocytic 6-MP) leukemiasPurine Analogs and Thioguanine Acute granulocytic, acute RelatedInhibitors (6-thioguanine; TG) lymphocytic and chronic granulocyticleukemias Pentostatin Hairy cell leukemia, mycosis (2-deoxycoformycin)fungoides, chronic lymphocytic leukemia Natural Vinca AlkaloidsVinblastine (VLB) Hodgkin's disease, non-Hodgkin's Products lymphomas,breast, testis Vincristine Acute lymphocytic leukemia, neuroblastoma,Wilms' tumor, rhabdomyosarcoma, Hodgkin's disease, non-Hodgkin'slymphomas, small-cell lung Epipodopyyllotoxins Etoposide Testis,small-cell lung and other lung, Tertiposide breast, Hodgkin's disease,non- Hodgkin's lymphomas, acute granulocytic leukemia, Kaposi's sarcomaAntibiotics Dactinomycin Choriocarcinoma, Wilms' tumor, (actinomycin D)rhabdomyosarcoma, testis, Kaposi's sarcoma Daunorubcin Acutegranulocytic and acute (daunomycin; lymphocytic leukemias rubidomycin)Doxorubicin Soft-tissue, osteogenic and other sarcomas; Hodgkin'sdisease, non- Hodgkin's lymphomas, acute leukemias, breast,genitourinary, thyroid, lung, stomach, neuroblastoma Bleomycin Testis,head and neck, skin, esophagus, lung and genitourinary tract; Hodgkin'sdisease, non- Hodgkin's lymphomas Plicamycin (mithramycin) Testis,malignant hypercalcemia Mitomycin (mitomycin C) Stomach, cervix, colon,breast, pancreas, bladder, head and neck Enzymes L-Asparaginase Acutelymphocytic leukemia Biological Response Interferon alfa Hairy cellleukemia., Kaposi's Modifiers sarcoma, melanoma, carcinoid, renal cell,ovary, bladder, non-Hodgkin's lymphomas, mycosis fungoides, multiplemyeloma, chronic granulocytic leukemia Platinum Coordination Cisplatin(cis-DDP) Testis, ovary, bladder, head and neck, Complexes Carboplatinlung, thyroid, cervix, endometrium, neuroblastoma, osteogenic sarcomaMiscellaneous Anthracenedione Mitoxantrone Acute granulocytic leukemia,breast Agents Substituted Urea Hydroxyurea Chronic granulocyticleukemia, polycythermia vera, essental thrombocytosis, malignantmelanoma Methyl Hydrazine Procarbazine Hodgkin's disease Derivative(N-methylhydrazine, MIH) Adrenocortical Mitotane(o,p′-DDD) Adrenalcortex Suppressant Aminoglutethimide Breast Hormones andAdrenocorticosteroids Prednisone (several other Acute and chroniclymphocytic Antagonists equivalent leukemias, non-Hodgkin's lymphomas,preparations available) Hodgkin's disease, breast ProgestinsHydroxyprogesterone Endometrium, breast caproate Medroxyprogesteroneacetate Magestrol acetate Estrogens Diethylstilbestrol Breast, prostateEthinyl estradiol (other preparations available) Antiestrogen TamoxifenBreast Androgens Testosterone propionate Breast Fluoxymesterone (otherpreparations available) Antiandrogen Flutamide ProstateGonadotropin-releasing Leuprolide Prostate Hormone analog

G2. Anti-Angiogenics

Under normal physiological conditions, humans or animals undergoangiogenesis only in very specific restricted situations. For example,angiogenesis is normally observed in wound healing, fetal and embryonicdevelopment and formation of the corpus luteum, endometrium andplacenta. Uncontrolled (persistent and/or unregulated) angiogenesis isrelated to various disease states, and occurs during tumor metastasis.

Both controlled and uncontrolled angiogenesis are thought to proceed ina similar manner. Endothelial cells and pericytes, surrounded by abasement membrane, form capillary blood vessels. Angiogenesis beginswith the erosion of the basement membrane by enzymes released byendothelial cells and leukocytes. The endothelial cells, which line thelumen of blood vessels, then protrude through the basement membrane.Angiogenic stimulants induce the endothelial cells to migrate throughthe eroded basement membrane. The migrating cells form a “sprout” offthe parent blood vessel, where the endothelial cells undergo mitosis andproliferate. The endothelial sprouts merge with each other to formcapillary loops, creating the new blood vessel.

The present VEGFR2-blocking, anti-VEGF antibody or 2C3-based inventionmay be used in combination with any one or more other anti-angiogenictherapies. Combinations with other agents that inhibit VEGF areincluded, such as other neutralizing antibodies (Kim et al., 1992;Presta et al., 1997; Sioussat et al., 1993; Kondo et al., 1993; Asano etal., 1995), soluble receptor constructs (Kendall and Thomas, 1993;Aiello et al., 1995; Lin et al., 1998; Millauer et al., 1996), tyrosinekinase inhibitors (Siemeister et al., 1998), antisense strategies, RNAaptamers and ribozymes against VEGF or VEGF receptors (Saleh et al.,1996; Cheng et al., 1996; Ke et al., 1998; Parry et al., 1999; eachincorporated herein by reference). Variants of VEGF with antagonisticproperties may also be employed, as described in WO 98/16551,specifically incorporated herein by reference.

The anti-angiogenic therapies may be based upon the provision of ananti-angiogenic agent or the inhibition of an angiogenic agent.Inhibition of angiogenic agents may be achieved by one or more of themethods described for inhibiting VEGF, including neutralizingantibodies, soluble receptor constructs, small molecule inhibitors,antisense, RNA aptamers and ribozymes may all be employed. For example,antibodies to angiogenin may be employed, as described in U.S. Pat. No.5,520,914, specifically incorporated herein by reference. In that FGF isconnected with angiogenesis, FGF inhibitors may also be used. Certainexamples are the compounds having N-acetylglucosamine alternating insequence with 2-O-sulfated uronic acid as their major repeating units,including glycosaminoglycans, such as archaran sulfate. Such compoundsare described in U.S. Pat. No. 6,028,061, specifically incorporatedherein by reference, and may be used in combination herewith.

Numerous tyrosine kinase inhibitors useful for the treatment ofangiogenesis, as manifest in various diseases states, are now known.These include, for example, the 4-aminopyrrolo[2,3-d]pyrimidines of U.S.Pat. No. 5,639,757, specifically incorporated herein by reference, whichmay also be used in combination with the present invention. Furtherexamples of organic molecules capable of modulating tyrosine kinasesignal transduction via the VEGFR2 receptor are the quinazolinecompounds and compositions of U.S. Pat. No. 5,792,771, which isspecifically incorporated herein by reference for the purpose ofdescribing further combinations for use with the present invention inthe treatment of angiogenic diseases.

Compounds of other chemical classes have also been shown to inhibitangiogenesis and may be used in combination with the present invention.For example, steroids such as the angiostatic 4,9(11)-steroids andC21-oxygenated steroids, as described in U.S. Pat. No. 5,972,922,specifically incorporated herein by reference, may be employed incombined therapy. U.S. Pat. Nos. 5,712,291 and 5,593,990, eachspecifically incorporated herein by reference, describe thalidomide andrelated compounds, precursors, analogs, metabolites and hydrolysisproducts, which may also be used in combination with the presentinvention to inhibit angiogenesis. The compounds in U.S. Pat. Nos.5,712,291 and 5,593,990 can be administered orally. Further exemplaryanti-angiogenic agents that are useful in connection with combinedtherapy are listed in Table D. Each of the agents listed therein areexemplary and by no means limiting.

TABLE D INHIBITORS AND NEGATIVE REGULATORS OF ANGIOGENESIS SubstancesReferences Angiostatin O'Reilly et al., 1994 Endostatin O'Reilly et al.,1997 16kDa prolactin fragment Ferrara et al., 1991; Clapp et al., 1993;D'Angelo et al., 1995; Lee et al, 1998 Laminin peptides Kleinman et al.,1993; Yamamura et al., 1993; Iwamoto et al., 1996; Tryggvason, 1993Fibronectin peptides Grant et al., 1998; Sheu et al., 1997 Tissuemetalloproteinase Sang, 1998 inhibitors (TIMP 1, 2, 3, 4) Plasminogenactivator inhibitors Soff et al., 1995 (PAI-1, -2) Tumor necrosis factorα (high Frater-Schroder et al., 1987 dose, in vitro) TGF-β1 RayChadhuryand D'Amore, 1991; Tada et al., 1994 Interferons (IFN-α, β, γ) Moore etal., 1998; Lingen et al., 1998 ELR- CXC Chemokines: Moore et al., 1998;Hiscox and Jiang, IL-12; SDF-1; MIG; Platelet 1997; Coughlin et al.,1998; Tanaka et factor 4 (PF-4); IP-10 al., 1997 Thrombospondin (TSP)Good et al., 1990; Frazier, 1991; Bornstein, 1992; Tolsma et al., 1993;Sheibani and Frazier, 1995; Volpert et al., 1998 SPARC Hasselaar andSage, 1992; Lane et al., 1992; Jendraschak and Sage, 19962-Methoxyoestradiol Fotsis et al., 1994 Proliferin-related proteinJackson et al., 1994 Suramin Gagliardi et al., 1992; Takano et al.,1994; Waltenberger et al., 1996; Gagliardi et al., 1998; Manetti et al.,1998 Thalidomide D'Amato et al., 1994; Kenyon et al., 1997 Wells, 1998Cortisone Thorpe et al., 1993 Folkman et al., 1983 Sakamoto et al., 1986Linomide Vukanovic et al., 1993; Ziche et al., 1998; Nagler et al., 1998Fumagillin (AGM-1470; TNP- Sipos et al., 1994; Yoshida et al., 1998 470)Tamoxifen Gagliardi and Collins, 1993; Lindner and Borden, 1997; Haranet al., 1994 Korean mistletoe extract Yoon et al., 1995 (Viscum albumcoloratum) Retinoids Oikawa et al., 1989; Lingen et al., 1996; Majewskiet al. 1996 CM101 Hellerqvist et al., 1993; Quinn et al., 1995; Wamil etal., 1997; DeVore et al., 1997 Dexamethasone Hori et al., 1996; Wolffetal., 1997 Leukemia inhibitory factor (LIF) Pepper et al., 1995

Certain preferred components for use in inhibiting angiogenesis areangiostatin, endostatin, vasculostatin, canstatin and maspin. Suchagents are described above in conjunction with the immunoconjugates ofthe present invention, but may be used in combined, but unconjugatedform. Other preferred agents also described above in immunoconjugateform are the angiopoietins, particularly angiopoietin-2, which iscontemplated for combined use with the present invention.

Certain anti-angiogenic therapies have already been shown to cause tumorregressions, including the bacterial polysaccharide CM101 and theantibody LM609. CM101 is a bacterial polysaccharide that has been wellcharacterized in its ability to induce neovascular inflammation intumors. CM101 binds to and cross-links receptors expressed ondedifferentiated endothelium that stimulates the activation of thecomplement system. It also initiates a cytokine-driven inflammatoryresponse that selectively targets the tumor. It is a uniquelyantipathoangiogenic agent that downregulates the expression VEGF and itsreceptors. CM101 is currently in clinical trials as an anti-cancer drug,and can be used in combination herewith.

Thrombospondin (TSP-1) and platelet factor 4 (PF4) may also be used incombination with the present invention. These are both angiogenesisinhibitors that associate with heparin and are found in plateleta-granules. TSP-1 is a large 450 kDa multi-domain glycoprotein that isconstituent of the extracellular matrix. TSP-1 binds to many of theproteoglycan molecules found in the extracellular matrix including,HSPGs, fibronectin, laminin, and different types of collagen. TSP-1inhibits endothelial cell migration and proliferation in vitro andangiogenesis in vivo. TSP-1 can also suppress the malignant phenotypeand tumorigenesis of transformed endothelial cells. The tumor suppressorgene p53 has been shown to directly regulate the expression of TSP-1such that, loss of p53 activity causes a dramatic reduction in TSP-1production and a concomitant increase in tumor initiated angiogenesis.

PF4 is a 70aa protein that is member of the CXC ELR-family of chemokinesthat is able to potently inhibit endothelial cell proliferation in vitroand angiogenesis in vivo. PF4 administered intratumorally or deliveredby an adenoviral vector is able to cause an inhibition of tumor growth.

Interferons and metalloproteinase inhibitors are two other classes ofnaturally occurring angiogenic inhibitors that can be combined with thepresent invention. The anti-endothelial activity of the interferons hasbeen known since the early 1980s, however, the mechanism of inhibitionis still unclear. It is known that they can inhibit endothelial cellmigration and that they do have some anti-angiogenic activity in vivothat is possibly mediated by an ability to inhibit the production ofangiogenic promoters by tumor cells. Vascular tumors in particular aresensitive to interferon, for example, proliferating hemangiomas can besuccessfully treated with IFNα.

Tissue inhibitors of metalloproteinases (TIMPs) are a family ofnaturally occurring inhibitors of matrix metalloproteases (MMPs) thatcan also inhibit angiogenesis and can be used in combined treatmentprotocols. MMPs play a key role in the angiogenic process as theydegrade the matrix through which endothelial cells and fibroblastsmigrate when extending or remodeling the vascular network. In fact, onemember of the MMPs, MMP-2, has been shown to associate with activatedendothelium through the integrin αvβ3 presumably for this purpose. Ifthis interaction is disrupted by a fragment of MMP-2, then angiogenesisis downregulated and in tumors growth is inhibited.

There are a number of pharmacological agents that inhibit angiogenesis,any one or more of which may be used in combination with the presentinvention. These include AGM-1470/TNP-470, thalidomide, andcarboxyamidotriazole (CAI). Fumagillin was found to be a potentinhibitor of angiogenesis in 1990, and since then the syntheticanalogues of fumagillin, AGM-1470 and TNP-470 have been developed. Bothof these drugs inhibit endothelial cell proliferation in vitro andangiogenesis in vivo. TNP-470 has been studied extensively in humanclinical trials with data suggesting that long-term administration isoptimal.

Thalidomide was originally used as a sedative but was found to be apotent teratogen and was discontinued. In 1994 it was found thatthalidomide is an angiogenesis inhibitor. Thalidomide is currently inclinical trials as an anti-cancer agent as well as a treatment ofvascular eye diseases.

CAI is a small molecular weight synthetic inhibitor of angiogenesis thatacts as a calcium channel blocker that prevents actin reorganization,endothelial cell migration and spreading on collagen IV. CAI inhibitsneovascularization at physiological attainable concentrations and iswell tolerated orally by cancer patients. Clinical trials with CAI haveyielded disease stabilization in 49% of cancer patients havingprogressive disease before treatment.

Cortisone in the presence of heparin or heparin fragments was shown toinhibit tumor growth in mice by blocking endothelial cell proliferation.The mechanism involved in the additive inhibitory effect of the steroidand heparin is unclear although it is thought that the heparin mayincrease the uptake of the steroid by endothelial cells. The mixture hasbeen shown to increase the dissolution of the basement membraneunderneath newly formed capillaries and this is also a possibleexplanation for the additive angiostatic effect. Heparin-cortisolconjugates also have potent angiostatic and anti-tumor effects activityin vivo.

Further specific angiogenesis inhibitors, including, but not limited to,Anti-Invasive Factor, retinoic acids and paclitaxel (U.S. Pat. No.5,716,981; incorporated herein by reference); AGM-1470 (Ingber et al.,1990; incorporated herein by reference); shark cartilage extract (U.S.Pat. No. 5,618,925; incorporated herein by reference); anionic polyamideor polyurea oligomers (U.S. Pat. No. 5,593,664; incorporated herein byreference); oxindole derivatives (U.S. Pat. No. 5,576,330; incorporatedherein by reference); estradiol derivatives (U.S. Pat. No. 5,504,074;incorporated herein by reference); and thiazolopyrimidine derivatives(U.S. Pat. No. 5,599,813; incorporated herein by reference) are alsocontemplated for use as anti-angiogenic compositions for the combineduses of the present invention.

Compositions comprising an antagonist of an o,03 integrin may also beused to inhibit angiogenesis in combination with the present invention.As disclosed in U.S. Pat. No. 5,766,591 (incorporated herein byreference), RGD-containing polypeptides and salts thereof, includingcyclic polypeptides, are suitable examples of α_(v)β₃ integrinantagonists

The antibody LM609 against the α_(v)β₃ integrin also induces tumorsregressions. Integrin (α_(v)β₃ antagonists, such as LM609, induceapoptosis of angiogenic endothelial cells leaving the quiescent bloodvessels unaffected. LM609 or other (α_(v)β₃ antagonists may also work byinhibiting the interaction of α_(v)β₃ and MMP-2, a proteolytic enzymethought to play an important role in migration of endothelial cells andfibroblasts. U.S. Pat. No. 5,753,230 is specifically incorporated hereinby reference to describe antibodies against α_(v)β₃ (vitronectinα_(v)β₃) for combined with the present invention for inhibitingangiogenesis.

Apoptosis of the angiogenic endothelium in this case may have a cascadeeffect on the rest of the vascular network. Inhibiting the tumorvascular network from completely responding to the tumor's signal toexpand may, in fact, initiate the partial or full collapse of thenetwork resulting in tumor cell death and loss of tumor volume. It ispossible that endostatin and angiostatin function in a similar fashion.The fact that LM609 does not affect quiescent vessels but is able tocause tumor regressions suggests strongly that not all blood vessels ina tumor need to be targeted for treatment in order to obtain ananti-tumor effect.

Other methods of therapeutic intervention based upon altering signalingthrough the Tie2 receptor can also be used in combination with thepresent invention, such as using a soluble Tie2 receptor capable ofblocking Tie2 activation (Lin et al., 1998). Delivery of such aconstruct using recombinant adenoviral gene therapy has been shown to beeffective in treating cancer and reducing metastases (Lin et al., 1998).

G3. Apoptosis4Inducing Agents

VEGFR2-blocking, anti-VEGF antibody or 2C3-based therapeutic agents mayalso be advantageously combined with methods to induce apoptosis.Various apoptosis-inducing agents have been described above inconnection with the immunoconjugates of the present invention. Any suchapoptosis-inducing agent may be used in combination with the presentinvention without being linked to an antibody of the invention.

Aside from the apoptosis-inducing agents described above asimmunoconjugates, a number of oncogenes have been identified thatinhibit apoptosis, or programmed cell death. Exemplary oncogenes in thiscategory include, but are not limited to, bcr-abl, .bcl-2 (distinct frombcl-1, cyclin D1; GenBank accession numbers M14745, X06487; U.S. Pat.Nos. 5,650,491; and 5,539,094; each incorporated herein by reference)and family members including Bcl-x1, Mcl-1, Bak, A1, A20. Overexpressionof bcl-2 was first discovered in T cell lymphomas. bcl-2 functions as anoncogene by binding and inactivating Bax, a protein in the apoptoticpathway. Inhibition of bcl-2 function prevents inactivation of Bax, andallows the apoptotic pathway to proceed.

Inhibition of this class of oncogenes, e.g., using antisense nucleotidesequences, is contemplated for use in the present invention to giveenhancement of apoptosis (U.S. Pat. Nos. 5,650,491; 5,539,094; and5,583,034; each incorporated herein by reference).

G4. Immunotoxins and Coaguligands

The treatment methods of the invention may be used in combination with[other] immunotoxins and/or coaguligands in which the targeting portionthereof, e.g., antibody or ligand, is directed to a relatively specificmarker of the tumor cells, tumor vasculature or tumor stroma. In commonwith the chemotherapeutic and anti-angiogenic agents discussed above,the combined use of targeted toxins or coagulants will generally resultin additive, markedly greater than additive or even synergisticanti-tumor results.

Generally speaking, antibodies or ligands for use in these additionalaspects of the invention will preferably recognize accessible tumorantigens that are preferentially, or specifically, expressed in thetumor site. The antibodies or ligands will also preferably exhibitproperties of high affinity; and the antibodies, ligands or conjugatesthereof, will not exert significant in vivo side effects againstlife-sustaining normal tissues, such as one or more tissues selectedfrom heart, kidney, brain, liver, bone marrow, colon, breast, prostate,thyroid, gall bladder, lung, adrenals, muscle, nerve fibers, pancreas,skin, or other life-sustaining organ or tissue in the human body. Theterm “significant side effects”, as used herein, refers to an antibody,ligand or antibody conjugate, that, when administered in vivo, willproduce only negligible or clinically manageable side effects, such asthose normally encountered during chemotherapy.

At least one binding region of these second anti-cancer agents employedin combination with the invention will be a component that is capable ofdelivering a toxin or coagulation factor to the tumor region, i.e.,capable of localizing within a tumor site. Such targeting agents may bedirected against a component of a tumor cell, tumor vasculature or tumorstroma. The targeting agents will generally bind to a surface-expressed,surface-accessible or surface-localized component of a tumor cell, tumorvasculature or tumor stroma. However, once tumor vasculature and tumorcell destruction begins, internal components will be released, allowingadditional targeting of virtually any tumor component.

Many tumor cell antigens have been described, any one which could beemployed as a target in connection with the combined aspects of thepresent invention. Appropriate tumor cell antigens for additionalimmunotoxin and coaguligand targeting include those recognized by theantibodies B3 (U.S. Pat. No. 5,242,813); incorporated herein byreference; ATCC HB 10573); KSI/4 (U.S. Pat. No. 4,975,369); incorporatedherein by reference; obtained from a cell comprising the vectors NRRLB-18356 and/or NRRL B-18357); 260F9 (ATCC HB 8488); and D612 (U.S. Pat.No. 5,183,756); incorporated herein by reference; ATCC HB 9796). One mayalso consult the ATCC Catalogue of any subsequent year to identify otherappropriate cell lines producing anti-tumor cell antibodies.

For tumor vasculature targeting, the targeting antibody or ligand willoften bind to a marker expressed by, adsorbed to, induced on orotherwise localized to the intratumoral blood vessels of a vascularizedtumor. Appropriate expressed target molecules include, for example,endoglin, E-selectin, P-selectin, VCAM-1, ICAM-1, PSMA (Liu et al.,1997), a TIE, a ligand reactive with LAM-1, a VEGF/VPF receptor, an FGFreceptor, α_(v)β₃ integrin, pleiotropin and endosialin. Suitableadsorbed targets are those such as VEGF, FGF, TGFβ, HGF, PF4, PDGF,TIMP, a ligand that binds to a TIE and tumor-associated fibronectinisoforms. Antigens naturally and artificially inducible by cytokines andcoagulants may also be targeted, such as ELAM-1, VCAM-1, ICAM-1, aligand reactive with LAM-1, endoglin, and even MHC Class II(cytokine-inducible, e.g., by IL-1, TNF-α, IFN-γIL4 and/or TNF-β); andE-selectin, P-selectin, PDGF and ICAM-1 (coagulant-inducible e.g., bythrombin, Factor IX/IXa, Factor X/Xa and/or plasmin).

The following patents and patent applications are specificallyincorporated herein by reference for the purposes of even furthersupplementing the present teachings regarding the preparation and use ofimmunotoxins directed against expressed, adsorbed, induced or localizedmarkers of tumor vasculature: U.S. application Ser. No. 08/482,369,Issue Fee paid Oct. 20, 1998; U.S. Pat. Nos. 5,855,866; 5,965,132;6,051,230; 6,004,555; 5,877,289; 6,004,554; 5,776,427; 5,863,538;5,660,827 and 6,036,955.

Further tumor vasculature targeting compositions and methods includethose targeting aminophospholipids, such as phosphatidylserine andphosphatidylethanolamine, recently discovered to be accessible, specificmarkers of tumor blood vessels. Administration of anti-aminophospholipidantibodies alone is sufficient to induce thrombosis and tumorregression. The present invention can thus be effectively combined withunconjugated, anti-phosphatidylserine and/or phosphatidylethanolamineantibodies; or immunoconjugates of such antibodies can be used.

The following provisional patent applications are specificallyincorporated herein by reference for the purposes of even furthersupplementing the present teachings regarding the preparation and use ofanti-aminophospholipid antibodies and immunotoxins: provisionalapplication Serial No. 60/092,672, filed Jul. 13, 1998, and provisionalapplication Serial No. 60/092,589, filed July 13, 1998. ApplicationSerial No. 60/092,589 is further incorporated herein by reference forthe purposes of further supplementing the present teachings regardingthe use of aminophospholipid binding protein conjugates, such as annexinconjugates, for use in delivering toxins and coagulants to tumor bloodvessels and for inducing thrombosis and tumor regression.

Suitable tumor stromal targets include components of the tumorextracellular matrix or stroma, or components those bound therein;including basement membrane markers, type IV collagen, laminin, heparansulfate, proteoglycan, fibronectins, activated platelets, LIBS andtenascin. A preferred target for such uses is RIBS.

The following patents and patent applications are specificallyincorporated herein by reference for the purposes of even furthersupplementing the present teachings regarding the preparation and use oftumor stromal targeting agents: U.S. applications Ser. No. 08/482,369(U.S. Pat. No. 6,903,399; Oct. 20, 1998); Ser. Nos. 08/485,482;08/487,427 (U.S. Pat. No. 6,004,555); Ser. No. 08/479,733 (U.S. Pat. No.5,877,289); Ser. Nos. 08/472,631; and 08/479,727 and 08/481,904 (U.S.Pat. No. 6,036,955).

The second anti-cancer therapeutics may be operatively attached to anyof the cytotoxic or otherwise anti-cellular agents described herein foruse in the VEGFR2-blocking, anti-VEGF antibody or 2C3-basedimmunotoxins. However, suitable anti-cellular agents also includeradioisotopes. Toxin moieties will be preferred, such as ricin A chainand deglycosylated A chain (dgA).

The second, targeted agent for optional use with the invention maycomprise a targeted component that is capable of promoting coagulation,i.e., a coaguligand. Here, the targeting antibody or ligand may bedirectly or indirectly, e.g., via another antibody, linked to any factorthat directly or indirectly stimulates coagulation, including any ofthose described herein for use in the VEGFR2-blocking, anti-VEGFantibody or 2C3-based coaguligands. Preferred coagulation factors forsuch uses are Tissue Factor (TF) and TF derivatives, such as truncatedTF (tTF), dimeric and multimeric TF, and mutant TF deficient in theability to activate Factor VII.

Effective doses of immunotoxins and coaguligands for combined use in thetreatment of cancer will be between about 0.1 mg/kg and about 2 mg/kg,and preferably, of between about 0.8 mg/kg and about 1.2 mg/kg, whenadministered via the IV route at a frequency of about 1 time per week.Some variation in dosage will necessarily occur depending on thecondition of the subject being treated. The physician responsible foradministration will determine the appropriate dose for the individualsubject.

G5. ADEPT and Prodrug Therapy

The VEGFR2-blocking, anti-VEGF antibody or 2C3-based antibodies of thepresent invention may be used in conjunction with prodrugs, wherein theVEGFR2-blocking. anti-VEGF antibody or 2C3-based antibody is operativelyassociated with a prodrug-activating component, such as aprodrug-activating enzyme, which converts a prodrug to the more activeform only upon contact with the antibody. This technology is generallytermed “ADEPT”, and is described in, e.g., WO 95/13095; WO 97/26918, WO97/24143, and U.S. Pat. No. 4,975,278 and 5,658,568, each specificallyincorporated herein by reference.

The term “prodrug”, as used herein, refers to a precursor or derivativeform of a biologically or pharmaceutically active substance that exertsreduced cytotoxic or otherwise anticellular effects on targets cells,including tumor vascular endothelial cells, in comparison to the parentdrug upon which it is based. Preferably, the prodrug or precursor formexerts significantly reduced, or more preferably, negligible, cytotoxicor anticellular effects in comparison to the “native” or parent form.“Prodrugs” are capable of being activated or converted to yield the moreactive, parent form of the drug.

The technical capability to make and use prodrugs exists within theskill of the ordinary artisan. Willman et al. (1986) and Stella et al.(1985) are each specifically incorporated herein by reference forpurposes of further supplementing the description and teachingconcerning how to make and use various prodrugs. Exemplary prodrugconstructs that may be used in the context of the present inventioninclude, but are not limited to, phosphate-containing prodrugs (U.S.Pat. No. 4,975,278), thiophosphate-containing prodrugs,sulfate-containing prodrugs, peptide-based prodrugs (U.S. Pat. Nos.5,660,829; 5,587,161; 5,405,990; WO 97/07118), D-amino acid-modifiedprodrugs, glycosylated prodrugs (U.S. Pat. Nos. 5,561,119; 5,646,298;4,904,768, 5,041,424), β-lactam-containing prodrugs, optionallysubstituted phenoxyacetamide-containing prodrugs (U.S. Pat. No.4,975,278), optionally substituted phenylacetamide-containing prodrugs,and even 5-fluorocytosine (U.S. Pat. No. 4,975,278) and 5-fluorouridineprodrugs and the like, wherein each of the patents are specificallyincorporated herein by reference.

The type of therapeutic agent or cytotoxic drug that can be used inprodrug form is virtually limitless. The more cytotoxic agents will bepreferred for such a form of delivery, over, e.g., the delivery ofcoagulants, which are less preferred for use as prodrugs. All that isrequired in forming the prodrug is to design the construct so that theprodrug is substantially inactive and the “released” or activated drughas substantial, or at least sufficient, activity for the intendedpurpose.

Various improvements on the original prodrugs are also known andcontemplated for use herewith, as disclosed in WO 95/03830; EP 751,144(anthracyclines); WO 97/07097 (cyclopropylindoles); and WO 96/20169. Forexample, prodrugs with reduced Km are described in U.S. Pat. No.5,621,002, specifically incorporated herein by reference, which may beused in the context of the present invention. Prodrug therapy that beconducted intracellularly is also known, as exemplified by WO 96/03151,specifically incorporated herein by reference, and can be practicedherewith.

For use in ADEPT, the agent that activates or converts the prodrug intothe more active drug is operatively attached to the VEGFR2-blocking,anti-VEGF antibody or 2C3-like antibody. The VEGFR2-blocking, anti-VEGFantibody or 2C3-like antibody thus localizes the prodrug convertingcapability within the angiogenic site, preferably, within the tumorvasculature and stroma, so that active drug is only produced in suchregions and not in circulation or in healthy tissues.

Enzymes that may be attached to VEGFR2-blocking, anti-VEGF antibody or2C3-based antibodies to function in prodrug activation include, but arenot limited to, alkaline phosphatase for use in combination withphosphate-containing prodrugs (U.S. Pat. No. 4,975,278); arylsulfatasefor use in combination with sulfate-containing prodrugs (U.S. Pat. No.5,270,196); peptidases and proteases, such as serratia protease,thermolysin, subtilisin, carboxypeptidase (U.S. Pat. Nos. 5,660,829;5,587,161; 5,405,990) and cathepsins (including cathepsin B and L), foruse in combination with peptide-based prodrugs;D-alanylcarboxypeptidases for use in combination with D-aminoacid-modified prodrugs; carbohydrate-cleaving enzymes such asβ-galactosidase and neuraminidase for use in combination withglycosylated prodrugs (U.S. Pat. Nos. 5,561,119; 5,646,298); β-lactamasefor use in combination with β-lactam-containing prodrugs; penicillinamidases, such as penicillin V amidase (U.S. Pat. No. 4,975,278) orpenicillin G amidase, for use in combination with drugs derivatized attheir amino nitrogens with phenoxyacetamide or phenylacetamide groups;and cytosine deaminase (U.S. Pat. Nos. 5,338,678; 5,545,548) for use incombination with 5-fluorocytosine-based prodrugs (U.S. Pat. No.4,975,278), wherein each of the patents are specifically incorporatedherein by reference.

Antibodies with enzymatic activity, known as catalytic antibodies or“abzymes”, can also be employed to convert prodrugs into active drugs.Abzymes based upon VEGFR2-blocking, anti-VEGF antibody or 2C3-likeantibodies thus form another aspect of the present invention. Thetechnical capacity to make abzymes also exists within one of ordinaryskill in the art, as exemplified by Massey et al. (1987), specificallyincorporated herein by reference for purposes of supplementing theabzyme teaching. Catalytic antibodies capable of catalyzing thebreakdown of a prodrug at the carbamate position, such as a nitrogenmustard aryl carbamate, are further contemplated, as described in EP745,673, specifically incorporated herein by reference.

H. Diagnostics and Imaging

The present invention further provides in vitro and in vivo diagnosticand imaging methods. Such methods are applicable for use in generatingdiagnostic, prognostic or imaging information for any angiogenicdisease, as exemplified by arthritis, psoriasis and solid tumors, butincluding all the angiogenic diseases disclosed herein. Outside thefield of tumor diagnostics and imaging, these aspects of the inventionare most preferred for use in in vitro diagnostic tests, preferablyeither where samples can be obtained non-invasively and tested in highthroughput assays and/or where the clinical diagnosis in ambiguous andconfirmation is desired.

H1. Immunodetection Methods and Kits

In still further embodiments, the present invention concernsimmunodetection methods for binding, purifying, removing, quantifying orotherwise generally detecting VEGF and for diagnosing angiogenicdiseases. The VEGFR2-blocking, anti-VEGF antibodies of the presentinvention, such as 2C3, may be employed to detect VEGF in vivo (seebelow), in isolated issue samples, biopsies or swabs and/or inhomogenized tissue samples. Such immunodetection methods have evidentdiagnostic utility, but also have applications to non-clinical samples,such as in the titering of antigen samples, and the like.

The steps of various useful immunodetection methods have been describedin the scientific literature, such as, e.g., Nakamura et al. (1987,incorporated herein by reference). In general, the immunobinding methodsinclude obtaining a sample suspected of containing VEGF and contactingthe sample with VEGFR2-blocking, anti-VEGF antibodies, such as 2C3,under conditions effective to allow the formation of immunocomplexes. Insuch methods, the antibody may be linked to a solid support, such as inthe form of a column matrix, and the sample suspected of containing VEGFwill be applied to the immobilized antibody.

More preferably, the immunobinding methods include methods for detectingor quantifying the amount of VEGF in a sample, which methods require thedetection or quantification of any immune complexes formed during thebinding process. Here, one would obtain a sample suspected of containingVEGF and contact the sample with an antibody in accordance herewith andthen detect or quantify the amount of immune complexes formed under thespecific conditions.

The biological sample analyzed may be any sample that is suspected ofcontaining VEGF, generally from an animal or patient suspected of havingan angiogenic disease. The samples may be a tissue section or specimen,a biopsy, a swab or smear test sample, a homogenized tissue extract orseparated or purified forms of such.

Contacting the chosen biological sample with the antibody underconditions effective and for a period of time sufficient to allow theformation of immune complexes (primary immune complexes) is generally amatter of simply adding an antibody composition to the sample andincubating the mixture for a period of time lone enough for theantibodies to form immune complexes with, i.e., to bind to, any VEGFpresent. After this time, the sample-antibody composition, such as atissue section, ELISA plate, dot blot or western blot, will generally bewashed to remove any non-specifically bound antibody species, allowingonly those antibodies specifically bound within the primary immunecomplexes to be detected.

The detection of immunocomplex formation is well known in the art andmay be achieved through the application of numerous approaches. Thesemethods are generally based upon the detection of a label or marker,such as any radioactive, fluorescent, biological or enzymatic tags orlabels known in the art. U.S. Patents concerning the use of such labelsinclude U.S. Pat. Nos. 3,817,837; 3,850,752; 3,939,350; 3,996,345;4,277,437; 4,275,149 and 4,366,241, each incorporated herein byreference. The use of enzymes that generate a colored product uponcontact with a chromogenic substrate are generally preferred. Secondarybinding ligand, such as a second antibody or a biotin/avidin ligandbinding arrangement, may also be used, as is known in the art.

The VEGFR2-blocking, anti-VEGF antibodies, such as 2C3, employed in thedetection may themselves be linked to a detectable label, wherein onewould then simply detect this label, thereby allowing the amount of theprimary immune complexes in the composition to be determined.

Preferably, the primary immune complexes are detected by means of asecond binding ligand that has binding affinity for the antibodies ofthe invention. In such cases, the second binding ligand may be linked toa detectable label. The second binding ligand is itself often anantibody, and may thus be termed a “secondary” antibody. The primaryimmune complexes are contacted with the labeled, secondary bindingligand, or antibody, under conditions effective and for a period of timesufficient to allow the formation of secondary immune complexes. Thesecondary immune complexes are then generally washed to remove anynon-specifically bound labeled secondary antibodies or ligands, and theremaining label in the secondary immune complexes is then detected.

Further methods include the detection of primary immune complexes by atwo step approach. A second binding ligand, such as an antibody, thathas binding affinity for the first antibody is used to form secondaryimmune complexes, as described above. After washing, the secondaryimmune complexes are contacted with a third binding ligand or antibodythat has binding affinity for the second antibody, again underconditions effective and for a period of time sufficient to allow theformation of immune complexes (tertiary immune complexes). The thirdligand or antibody is linked to a detectable label, allowing detectionof the tertiary immune complexes thus formed. This system may providefor signal amplification if desired.

In the clinical diagnosis or monitoring of patients with an angiogenicdisease, the detection of VEGF, or an increase in the levels of VEGF, incomparison to the levels in a corresponding biological sample from anormal subject is indicative of a patient with an angiogenic disease.

However, as is known to those of skill in the art, such a clinicaldiagnosis would not likely be made on the basis of this method inisolation. Those of skill in the art are very familiar withdifferentiating between significant expression of a biomarker, whichrepresents a positive identification, and low level or backgroundexpression of a biomarker. Indeed, background expression levels areoften used to form a “cut-off′ above which increased staining will bescored as significant or positive.

H2. Imaging

These aspects of the invention are preferred for use in tumor imagingmethods and combined tumor treatment and imaging methods.VEGFR2-blocking, anti-VEGF antibodies or 2C3-based antibodies that arelinked to one or more detectable agents are envisioned for use inimaging per se, or for pre-imaging the tumor to form a reliable imageprior to treatment. Such compositions and methods can also be applied tothe imaging and diagnosis of any other angiogenic disease or condition,particularly non-malignant tumors, atherosclerosis and conditions inwhich an internal image is desired for diagnostic or prognostic purposesor to design treatment.

VEGFR2-blocking, anti-VEGF antibody or 2C3-based imaging antibodies willgenerally comprise a VEGFR2-blocking, anti-VEGF antibody or 2C3-basedantibody operatively attached, or conjugated to, a detectable label.“Detectable labels” are compounds or elements that can be detected dueto their specific functional properties, or chemical characteristics,the use of which allows the component to which they are attached to bedetected, and further quantified if desired. In antibody conjugates forin vivo diagnostic protocols or “imaging methods” labels are requiredthat can be detected using non-invasive methods.

Many appropriate imaging agents are known in the art, as are methods fortheir attachment to antibodies and binding ligands (see, e.g., U.S. Pat.Nos. 5,021,236 and 4,472,509, both incorporated herein by reference).Certain attachment methods involve the use of a metal chelate complexemploying, for example, an organic chelating agent such a DTPA attachedto the antibody (U.S. Pat. No. 4,472,509). Monoclonal antibodies mayalso be reacted with an enzyme in the presence of a coupling agent suchas glutaraldehyde or periodate. Conjugates with fluorescein markers areprepared in the presence of these coupling agents or by reaction with anisothiocyanate.

An example of detectable labels are the paramagnetic ions. In this case,suitable ions include chromium (III), manganese (II), iron (III), iron(II), cobalt (II), nickel (II), copper (II), neodymium (III), samarium(III), ytterbium (III), gadolinium (III), vanadium (II), terbium (III),dysprosium (III), holmium (III) and erbium (III), with gadolinium beingparticularly preferred.

Ions useful in other contexts, such as X-ray imaging, include but arenot limited to lanthanum (III), gold (III), lead (II), and especiallybismuth (III). Fluorescent labels include rhodamine, fluorescein andrenographin. Rhodamine and fluorescein are often linked via anisothiocyanate intermediate.

In the case of radioactive isotopes for diagnostic applications,suitable examples include ¹⁴carbon, ⁵¹chromium, ³⁶chlorine, ⁵⁷cobalt,⁵⁷cobalt, copper, ¹⁵²Eu, gallium⁶⁷, ³hydrogen, iodine¹²³, iodine¹²⁵,iodine¹³¹, indium^(131,) ⁵⁹iron, ³²phosphorus, rhenium¹⁸⁶, rhenium ¹⁸⁸,⁷⁵selenium, ³⁵sulphur, technetium^(99m) and yttrium⁹⁰. ¹²⁵I is oftenbeing preferred for use in certain embodiments, and technicium^(99m) andindium¹¹¹ are also often preferred due to their low energy andsuitability for long range detection.

Radioactively labeled VEGFR2-blocking, anti-VEGF antibody or 2C3-basedantibodies for use in the present invention may be produced according towell-known methods in the art. For instance, intermediary functionalgroups that are often used to bind radioisotopic metallic ions toantibodies are diethylenetriaminepentaacetic acid (DTPA) and ethylenediaminetetracetic acid (EDTA).

Monoclonal antibodies can also be iodinated by contact with sodium orpotassium iodide and a chemical oxidizing agent such as sodiumhypochlorite, or an enzymatic oxidizing agent, such as lactoperoxidase.Antibodies according to the invention may be labeled with technetium-⁹⁹mby ligand exchange process, for example, by reducing pertechnate withstannous solution, chelating the reduced technetium onto a Sephadexcolumn and applying the antibody to this column; or by direct labelingtechniques, e.g., by incubating pertechnate, a reducing agent such asSNCl₂, a buffer solution such as sodium-potassium phthalate solution,and the antibody.

Any of the foregoing type of detectably labeled VEGFR2-blocking,anti-VEGF antibody or 2C3-based antibodies may be used in the imaging orcombined imaging and treatment aspects of the present invention. Theyare equally suitable for use in in vitro diagnostics. Dosages for invivo imaging embodiments are generally less than for therapy, but arealso dependent upon the age and weight of a patient. One time dosesshould be sufficient.

The in vivo diagnostic or imaging methods generally compriseadministering to a patient a diagnostically effective amount of aVEGFR2-blocking, anti-VEGF antibody or 2C3-based antibody that isconjugated to a marker that is detectable by non-invasive methods. Theantibody-marker conjugate is allowed sufficient time to localize andbind to VEGF within the tumor. The patient is then exposed to adetection device to identify the detectable marker, thus forming animage of the tumor.

H3. Diagnostic Kits

In still further embodiments, the present invention provides diagnostickits, including both immunodetection and imaging kits, for use with theimmunodetection and imaging methods described above. Accordingly, theVEGFR2-blocking, anti-VEGF antibodies, such as 2C3, are provided in thekit, generally comprised within a suitable container.

For immunodetection, the antibodies may be bound to a solid support,such as a well of a microtitre plate, although antibody solutions orpowders for reconstitution are preferred. The immunodetection kitspreferably comprise at least a first immunodetection reagent. Theimmunodetection reagents of the kit may take any one of a variety offorms, including those detectable labels that are associated with orlinked to the given antibody. Detectable labels that are associated withor attached to a secondary binding ligand are also contemplated.Exemplary secondary ligands are those secondary antibodies that havebinding affinity for the first antibody.

Further suitable immunodetection reagents for use in the present kitsinclude the two-component reagent that comprises a secondary antibodythat has binding affinity for the first antibody, along with a thirdantibody that has binding affinity for the second antibody, the thirdantibody being linked to a detectable label. As noted above, a number ofexemplary labels are known in the art and all such labels may beemployed in connection with the present invention. These kits maycontain antibody-label conjugates either in fully conjugated form, inthe form of intermediates, or as separate moieties to be conjugated bythe user of the kit.

The imaging kits will preferably comprise a VEGFR2-blocking, anti-VEGFantibody, such as 2C3, that is already attached to an in vivo detectablelabel. However, the label and attachment means could be separatelysupplied.

Either kit may further comprise control agents, such as suitablyaliquoted compositions of VEGF, whether labeled or unlabeled, as may beused to prepare a standard curve for a detection assay. The componentsof the kits may be packaged either in aqueous media or in lyophilizedform.

The container means of the kits will generally include at least onevial, test tube, flask, bottle, syringe or other container means, intowhich the antibody or antigen may be placed, and preferably, suitablyaliquoted. Where a second or third binding ligand or additionalcomponent is provided, the kit will also generally contain a second,third or other additional container into which this ligand or componentmay be placed. The kits may also include other diagnostic reagents foruse in the diagnosis of any one or more angiogenic diseases. Preferably,second diagnostics not based upon VEGF binding will be used.

The kits of the present invention will also typically include a meansfor containing the antibody, and any other reagent containers in closeconfinement for commercial sale. Such containers may include injectionor blow-molded plastic containers into which the desired vials areretained.

The following examples are included to demonstrate preferred embodimentsof the invention. It should be appreciated by those of skill in the artthat the techniques disclosed in the examples which follow representtechniques discovered by the inventor to function well in the practiceof the invention, and thus can be considered to constitute preferredmodes for its practice. However, those of skill in the art should, inlight of the present disclosure, appreciate that many changes can bemade in the specific embodiments which are disclosed and still obtain alike or similar result without departing from the spirit and scope ofthe invention.

EXAMPLE I Generation and Unique Characteristics of Anti-VEGF Antibody2C3

A. Materials and Methods

1. Immunogens

Peptides corresponding to the N-terminal 26 amino acids of human VEGF(huVEGF; SEQ ID NO:10) and the N-terminal 25 amino acids of guinea pigVEGF (gpVEGF; SEQ ID NO:11) were synthesized by the Biopolymers Facilityof the Howard Hughes Medical Institute at UT Southwestern Medical Centerat Dallas. The peptides had the following sequences (N to C):

APMAEGGGQNHHEVVKFMDVYQRSYC; SEQ ID NO:10; and

APMAEGEQKPREVVKFMDVYKRSYC; SEQ ID NO: 11.

Peptides were conjugated via the C-terminal cysteine to thyroglobulinusing succinimidyl 4-(N-maleimidomethyl) cyclohexane-1-carboxylate(SMCC) linker (Pierce, Rockford, Ill.). Control conjugates were alsoprepared that consisted of L-cysteine linked to thyroglobulin.Conjugates were separated from free peptide or linker by size exclusionchromatography.

Recombinant human VEGF was also separately used as an immunogen(obtained from Dr. S. Ramakrishnan, University of Minnesota,Minneapolis, Minn.).

2. Hybridomas

For the production of anti-gpVEGF antibody producing hybridomas,C57/B1-6 mice were immunized with the gpVEGF-peptide-thyroglobulinconjugate in TiterMax adjuvant (CytRX Co., Norcross, GA). For theproduction of anti-human VEGF antibodies, BALB/c mice were immunizedwith either the huVEGF-peptide-thyroglobulin conjugate or recombinanthuman VEGF in TiterMax. Three days after the final boost spleenocyteswere fused with myeloma P3X63AG8.653 (American Type Culture Collection,Rockville, Md.) cells and were cultured as described by Morrow et al(1990; incorporated herein by reference).

3. Antibody Purification

IgG antibodies (2C3, 12D7, 3E7) were purified from tissue culturesupernatant by ammonium sulfate precipitation and Protein Achromatography using the Pierce ImmunoPure Binding/Elution bufferingsystem (Pierce).

IgM antibodies (GV39M, 11B5, 7G3) were purified from tissue culturesupernatant by 50% saturated ammonium sulfate precipitation,resuspension of the pellet in PBS (pH 7.4) and dialysis against dH₂O toprecipitate the euglobulin. The dH₂O precipitate was resuspended in PBSand fractionated by size-exclusion chromatography on a Sepharose S300column (Pharmacia). The IgM fraction was 85-90% pure, as judged bySDS-PAGE.

4. Control Antibodies

Various control antibodies have been used throughout these studiesincluding mAb 4.6.1 (mouse anti-human VEGF from Genentech, Inc.), Ab-3(mouse anti-human VEGF from OncogeneScience, Inc.), A-20 (rabbitanti-human VEGF from Santa Cruz Biotechnology, Inc., Santa Cruz,Calif.), OX7 (mouse anti-rat Thyl.1 from Dr. A. F. Williams, MRCCellular Immunology Unit, Oxford, UK), MTSA (a mouse myeloma IgM ofirrelevant specificity from Dr. E. S. Vitetta, UT-Southwestern, Dallas,Tex.), 1A8 (mouse anti-mouse Flk-1; Philip E. Thorpe and colleagues),MECA 32 (rat anti-mouse endothelium from Dr. E. Butcher, StanfordUniversity, Stanford, Calif.), and TEC 11 (mouse anti-human endoglin;U.S. Pat. No. 5,660,827).

5. Initial Screening

For the initial screening, 96-well ELISA plates (Falcon, Franklin Lakes,N.J.) were coated with 250 ng of either the VEGF peptide orVEGF-Cys-thyroglobulin conjugate and blocked with 5% casein acidhydrolysate (Sigma, St. Louis, Mo.). Supernatants from the anti-gpVEGFhybridomas and the initial anti-human VEGF hybridomas were screened onthe antigen coated plates through a dual indirect ELISA technique(Crowther, 1995).

Hybridomas that showed preferential reactivity with VEGFpeptide-thyroglobulin but no or weak reactivity with Cys-thyroglobulinwere further screened through immunohistochemistry (described below) onfrozen sections of tumor tissue.

6. Immunohistochemistry

Guinea pig line 10 hepatocellular carcinoma tumor cells (obtained fromDr. Ronald Neuman, NIH, Bethesda, Md.) were grown in strain 2 guineapigs (NCI, Bethesda, Md.). The human tumors NCI-H358 non-small cell lungcarcinoma (NSCLC), NCI-H460 NSCLC (both obtained from Dr. Adi Gazdar, UTSouthwestern, Dallas, Tex.), HT29 colon adenocarcinoma (American TypeCulture Collection), and L540CY Hodgkin's lymphoma (obtained fromProfessor V. Diehl, Cologne, Germany) were grown as xenografts in CB17SCID mice (Charles River, Wilmington, Mass.).

Tumors were snap frozen in liquid nitrogen and stored at −70° C. Frozensamples of tumor specimens from patients were obtained from the NationalCancer Institute Cooperative Human Tissue Network (Southern Division,Birmingham, Ala.). Immunohistochemistry was performed as described byBurrows et al. (1995).

7. ELISA Analysis

Hybridoma supernatants from animals immunized with VEGF were screenedthrough a differential indirect ELISA technique employing threedifferent antigens: human VEGF alone, VEGF:Flk-1/SEAP complex, andFlk-1/SEAP alone. For the human VEGF alone, certain ELISA plates werecoated with 100 ng of VEGF.

For Flk-1/SEAP alone, other ELISA plates were coated with 500 ng ofFlk-1/SEAP, a soluble form of the mouse VEGF receptor (cells secretingFlk-1/SEAP were obtained from Dr. Ihor Lemischka, Princeton University,Princeton, N.J.). The Flk-1/SEAP protein was produced and purified asdescribed by Tessler et al. (1994). Basically, the extracellular domainof Flk-1 (sFlk-1) was produced in Spodoptera frugiperda (Sf9) cells andpurified by immunoaffinity techniques utilizing a monoclonal anti-Flk-1antibody (1A8). sFlk-1 was then biotinylated and bound on avidin-coatedplates.

To prepare plates coated with VEGF:Flk-1/SEAP complex, purified sFlk-1was biotinylated and reacted with VEGF overnight at 4° C. in bindingbuffer (10 mM HEPES, 150 mM NaCl, 20 μml bovine serum albumin and 0.1μg/ml heparin) at a molar ratio of sFlk-1 to VEGF of 2.5:1 to encouragedimer formation. The VEGF:sFlk-1 complex was then incubated in avidincoated wells of a 96 well microtiter plate to produce plates coated withVEGF associated with its receptor.

The reactivity of the antibodies with VEGF alone, biotinylated sFlk-1and VEGF:sFLk-1 complex was then determined in controlled studies usingthe three antigens on avidin-coated plates. The reactivity wasdetermined as described above for the initial screening.

A capture ELISA was also developed. In the capture ELISA, microtiterplates were coated overnight at 4° C. with 100 ng of the indicatedantibody. The wells were washed and blocked as above, then incubatedwith various concentrations of biotinylated VEGF or VEGF:sFlk-1-biotin.Streptavidin conjugated to peroxidase (Kirkegaard & Perry Laboratories,Inc.), diluted 1:2000, was used as a second layer and developed.

Competition ELISA studies were performed by first labeling theantibodies with peroxidase according to the manufacturer's instructions(EZ-Link Activated Peroxidase, Pierce). The antigen used for thecompetition studies with 12D7, 3E7, 2C3, and 7G3 was VEGF-biotincaptured by avidin on an ELISA plate. Approximately 0.5-2.0 μg/ml ofperoxidase labeled test antibody was incubated on the plate in thepresence of either buffer alone, an irrelevant IgG, or the otheranti-VEGF competing antibodies in a 10-100 fold excess.

The binding of the labeled antibody was assessed by addition of3,3′5,5′-tetramethylbenzidine (TMB) substrate (Kirkegaard and PerryLaboratories, Inc). Reactions were stopped after 15 min with 1M H₃PO₄and read spectrophotometrically at 450 nM. The assay was done intriplicate at least twice for each combination of labeled and competitorantibody. Two antibodies were considered to be in the same epitope groupif they cross-blocked each other's binding by greater than 80%.

GV39M and 11B5 did not retain binding activity after peroxidase labelingbut tolerated biotinylation. GV39M and 11B5 were biotinylated and testedagainst VEGF:sFlk-1 that had either been captured by the anti-Flk-1antibody (1A8) or coated directly on an ELISA plate.

8. Western Blot Analysis

Purified recombinant VEGF in the presence of 5% fetal calf serum wasseparated by 12% SDS-PAGE under reducing and non-reducing conditions andtransferred to nitrocellulose. The nitrocellulose membrane was blockedusing Sea-Block PP8241 (East Coast Biologics, Berwick, Me.), and probedwith primary antibodies using a mini-blotter apparatus (Immunetics,Cambridge, Mass.). The membranes were developed after incubation withthe appropriate peroxidase-conjugated secondary antibody by ECL enhancedchemiluminescence.

B. RESULTS

1. 2C3 has a Unique Epitope Specificity

Table 1 summarizes information on the class/subclass of differentanti-VEGF antibodies, the epitope groups that they recognize on VEGF,and their preferential binding to VEGF or VEGF:receptor (VEGF:Flk-1)complex. In all instances the antibodies bound to VEGF121 and VEGF165equally well and produced essentially the same results. The resultsbelow are for VEGF165 unless stipulated otherwise.

TABLE 1 SUMMARY OF ANTI-VEGF ANTIBODY PROPERTIES Epitope VEGF Group¹Clone Isotype Immunogen² Predominant Reactivity³ 1 GV39M IgM,k GpN-terminus VEGF:Flk-1 1 11B5 IgM,k Hu N-terminus VEGF:Flk-1 2 3E7 IgG1,1Hu N-terminus VEGF and VEGF:Flk-1 2 7G3 IgM,k Hu N-terminus VEGF andVEGF:Flk-1 3 12D7 IgG1,k Hu N-terminus VEGF 4 2C3 IgG2a,k rHuVEGF VEGF⁴centered A4.6.1 IgG1 VEGF around aa 89-94 ¹Epitope groups weredetermined through competitive ELISA. ²Mice were immunized with asynthetic peptide corresponding to either the N-terminal 26 amino acidsof human VEGF (11B5, 3E7, 7G3, and 12D7), the N-terminal 25 amino acidsof guinea pig VEGF (GV39M), or with full length recombinant human VEGF(2C3). ³The antibodies were screened in an indirect and a capture ELISAfor reactivity with VEGF alone or with VEGF associated with sFlk-1(VEGF:Flk-1). ⁴A4.6.1 has precisely defined epitope, which is distinctfrom epitope Group 4 recognized by 2C3. The A4.6.1 studies are reportedin Kim et al., 1992; Wiesmann et al., 1997; Muller et al., 1998; andKeyt et al., 1996, each incorporated herein by reference.

Competitive binding studies using biotinylated or peroxidase-labeledtest antibodies and a 10-100 fold excess of unlabeled competingantibodies showed that 2C3 binds to a unique eptiope. These studiesfirst revealed that GV39M and 11BS cross-blocked each other's binding tpVEGF:Flk-1, and that 3E7 and 7G3 cross-blocked each other's binding toVEGF-biotin captured onto avidin. GV39M and 11B5 were arbitrarilyassigned to epitope group 1. while 3E7G3 were assigned to epitope group2.

2C3 and the remaining antibody, 12D7, did not interfere significantlywith each other's binding or the binding of the rest of the antibodiesto VEGF or VEGF:receptor. 12D7 was assigned to epitope group 3, and 2C3was assigned to epitope group 4 (Table 1).

As tabulated above, 2C3 sees a different epitope to the antibody A4.6.1.The inventors' competition studies showed that 2C3 and A4.6.1 are notcross-reactive. The epitope recognized by A4.6.1 has also been preciselydefined and is a continuous epitope centered around amino acids 89-94(Kim et al, 1992; Wiesmann et al., 1997; Muller et al,1998; Keyt et al.,1996; each incorporated herein by reference). There are also a numberknown differences between 2C3 and A4.6.1 (see below).

2. 2C3 Can Bind to Free VEGF

There were marked differences in the ability of the antibodies to bindto soluble VEGF in free and complexed form (Table 2). These studiesprovide further evidence of the unique nature of 2C3. Table 2 shows thatGV39M and llB5 display a strong preference for the VEGF:receptorcomplex, with half-maximal binding being attained with VEGF:Flk-1 at 5.5and 2 nM respectively as compared with 400 and 800 nM respectively forfree VEGF in solution.

In contrast, 2C3 and 12D7 displayed a preference for free VEGF, withhalf-maximal binding being attained at 1 and 20 nM respectively ascompared with 150 and 250 nM respectively for the VEGF:Flk-1 complex.However, 2C3 localizes to tumor vasculature, as well as tumor stroma,after injection in vivo (see below).

3E7 bound equally well to free VEGF and the VEGF:Flk-1 complex withhalf-maximal binding being attained at 1 nM for both.

TABLE 2 ELISA CAPTURE OF VEGF vs. VEGF:FLK-1 Concentration giving 50%maximal binding (nM)¹ Ratio of Clone VEGF VEGF:Flk-1 VEGF/VEGF:Flk-1²GV39M 400*   5.5 72.7 11B5 800*  2 400.0 3E7   0.9  1 0.9 12D7 20 250*0.1 2C3  1 150  0.007 Mab4.6.1³ 0.3 500* 0.0006 1A8 NR⁴   1.5 ControlNR  600* *Extrapolated value ¹Half-maximal binding values weredetermined by titrating biotinylated VEGF and biotinylated sFlk-1complexed with VEGF in triplicate onto wells coated with the indicatedantibody and then developing with peroxidase-labeled avidin. ²Ratiosgreater than 1.0 indicate a preference of antibody for complex(VEGF-Flk-1) while ratios less than 1.0 indicate a preference for VEGF.³Control antibodies used included; 1A8 (mouse anti-Flk-1), Mab 4.6.1(mouse anti-human VEGF from Genentech), and an irrelevant IgM as anegative control. ⁴NR = no reaction detected.

3. 2C3 Recognizes a Non-Conformationally-Dependent Epitope

Western blot analysis shows that 12D7, 2C3 and 7G3 react with denaturedVEGF121 and VEGF 165 under reducing and non-reducing conditions. Theseantibodies therefore appear to recognize epitopes that are notconformationally-dependent.

In contrast, GV39M, 11B5, and 3E7 did not react with VEGF on westernblots, possibly because they recognize an epitope on the N-terminus ofVEGF that is conformationally-dependent and is distorted underdenaturing conditions.

Western blot analyses of anti-VEGF antibodies were conducted byseparating VEGF165 in the presence of 5% FCS using SDS-PAGE on a 12% geland analyzing by a standard western blotting protocol using ECLdetection. The primary antibodies were incubated with the nitrocellulosemembrane using a multi-lane mini-blotter apparatus. Control antibodiesincluded: Ab-3, a monoclonal IgG specific for VEGF from Oncogene Scienceat 1 μg/ml, A-20, a rabbit anti-VEGF antibody from Santa CruzBiotechnology, Inc. at 5 μg/ml, and an IgG of irrelevant specificity at10 μg/ml.

A typical western blot for the different antibodies, including 2C3 at5gg/ml, showed dimeric VEGF as a large band at approximately 42 kd. Amultimer of VEGF at approximately 130 kd was also evident with 12D7,7G3, and a positive control antibody.

4. Tumor Immunohistochemistry

Tumors examined through immunohistochemistry were human tumors ofvarious types from cancer patients, transplantable human tumorxenografts of various types grown in mice, guinea pig Line 10 tumorgrown in guinea pig, and mouse 3LL tumor grown in mice (see legend toTable 3 for details).

The immunohistochemical reactivity of 3E7, GV39M, and 11B5 on NCI-H358human NSCLC xenografts was determined and compared with controlantibodies (an IgG of irrelevant specificity; A-20, a rabbit anti-VEGFantibody; and MECA 32, a rat anti-mouse endothelial cell antibody). 8 μmfrozen sections of NCI-H358 human NSCLC grown in SCID mice were stainedusing an indirect immunoperoxidase technique and were counterstainedwith hematoxylin.

It was determined that GV39M and 11B5, which recognize epitope group 1on VEGF, stained vascular endothelial cells strongly and perivascularconnective tissue moderately in all tumors examined. The epitope group 1antibodies differed in their reactivity with tumor cells, in that GV39Mreacted only weakly with tumor cells while 11B5 reacted more strongly.Approximately 80% of endothelial cells that were stained by MECA 32(mouse) or TEC 11 (human) were also stained by GV39M and 11B5.

3E7 and 7G3, which recognize VEGF epitope group 2, showed reactivitywith vascular endothelial cells, connective tissue, and tumor cells inall tumors examined (Table 3). The intensity of endothelial cellstaining was typically stronger than the tumor cell or connective tissuestaining, especially when the antibodies were applied at low (1-2 μg/ml)concentrations where there was a noticeably increased selectivity forvascular endothelium.

TABLE 3 IMMUNOHISTOCHEMICAL REACTIVITY OF ANTI-VEGF ANTIBODIES ON TUMORSECTIONS Endothelial Cell Staining Guinea Pig Mouse Xenograft³ Hu Tumor⁴Tumor⁵ Tumor⁶ Group Clone¹ Reactivity² (various) (various) (Line 10)(3LL) 1 GV39M EC > CT > TC 3-4+ 2-3+ 4+ 3+ 1 11B5 EC > CT = TC 3+ 3+ 3+3+ 2 3 E7 EC > CT = TC 2+ 2+ 2+ 1-2+ 2 7G3 EC > CT = TC 3+ 2-3+ 3+ 2+ 312D7 NR − − − − 4 2C3 NR − − − — Immunohistochemical analysis wasperformed on acetone fixed frozen sections of tumor tissues throughstandard immunohistochemical techniques. The sections were examinedmicroscopically and scored for reactivity as follows: −, negative; +/−,very weak; 1+, weak; 2+, moderate; 3+, strong; 4+, very strong. ¹2C3 and12D7 were applied at 20 μg/ml; all other antibodies were at 5-10 μg/ml.²Reactivity definitions: EC = endothelium; CT = connective tissue; TC =tumor cell; NR = no reaction ³Human tumor xenografts tested; NCI-H358NSCLC, NCI-H460 NSCLC, HT29 colon adenocarcinoma, L540 Hodgkin'slymphoma. ⁴Human tumors tested; Soft tissue sarcoma, Hodgkin's lymphoma,Renal, Breast, Parotid, Colon, Lung, and Endometrial carcinomas.⁵Reactivity with guinea pig VEGF in line 10 guinea pig tumor sections.⁶Reactivity with mouse VEGF in mouse 3LL Lewis Lung carcinoma tumorsections.

12D7 and 2C3 did not stain frozen sections of any tumor tissues,probably because acetone fixation of the tissue destroyed antibodybinding. However, 2C3 localized to tumor tissue after injection in vivo(see below).

GV39M, 11B5, 3E7 and 7G3 reacted with rodent vasculature on frozensections of guinea pig line 10 tumor grown in guinea pigs and mouse 3LLtumor grown in mice. GV39M, 11B5, and 7G3 reacted as strongly withguinea pig and mouse tumor vasculature as they did with humanvasculature in human tumor specimens. 3E7 stained the mouse 3LL tumorless intensely than it did the guinea pig or human tumor sections,suggesting that 3E7 has a lower affinity for mouse VEGF. These resultsaccord with analysis by indirect ELISA, which has shown that all theantibodies except 2C3 react with mouse VEGF.

EXAMPLE II 2C3 Inhibits Endothelial Cell Migration

A. Materials and Methods

Endothelial Cell Growth Assay

Adult bovine aortic endothelial (ABAE) cells were plated into 96-welltissue culture plates at 1500 cells/well and grown in the presence of0.5 nM human VEGF with the addition of the various sample and controlantibodies. Control wells received media with or without VEGF.

After 4 days of incubation, the cells were quantified by an MTS(3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxylmethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium,inner salt) conversion assay, where MTS conversion to a formazan isproportional to cell number and can be followed by absorbance at 490 nM(Cell Titer 96 AQueous One Solution Cell Proliferation Assay, Promega,Madison, WI). The assay was performed according to the manufacturer'sinstructions.

Cell growth was estimated by subtracting the MTS conversion in culturesto which VEGF was not added. Results were expressed as a percentage ofthe MTS conversion in control cultures to which only VEGF was added(Buttke et al., 1993).

B. Results

Inhibition of VEGF-Mediated Endothelial Cell Growth

The IgG antibodies 3E7 and 12D7, recognizing epitope groups 1-3 on VEGF,did not inhibit VEGF-mediated growth of ABAE cells (FIG. 1), suggestingthat they are non-blocking anti-VEGF antibodies whose epitopes are notinvolved in the VEGF:KDR interaction. The IgM antibody GV39M, alsorecognizing epitope groups 1-3 on VEGF, likewise did not inhibitVEGF-mediated growth of ABAE cells and is a non-blocking anti-VEGFantibody.

In contrast, 2C3 against epitope 4 on VEGF and a reference neutralizinganti-VEGF antibody, Mab 4.6.1, inhibited VEGF-mediated ABAE growth by50% at 3 nM and 1 nM respectively (FIG. 1). This indicates that 2C3 canneutralize the mitogenic activity of VEGF.

The definition of 2C3 as blocking Mab distinguishes 2C3 from a range ofother antibodies in addition to GV39M, 3E7 and 12D7. Various anti-VEGFantibodies, such as Ab-3, are known to be non-blocking monoclonals,which are clearly distinct from 2C3.

One of the IgM antibodies, 11B5, was toxic to ABAE cells at aconcentration of 8 nM or greater. The cells detached within 30 min andwithin 24 h took up trypan blue dye. This effect appears to be cell typespecific since HUVEC, porcine aortic endothelial cells, and bEND.3 cellswere unaffected by 11B5 even at 40 nM. The toxic effect of 11B5 appearsto be growth factor-independent as it occurred in the absence of addedVEGF and in the presence of basic fibroblast growth factor (bFGF).

EXAMPLE III 2C3 Specifically Localizes to Tumors In Vivo

A. Materials and Methods

In Vivo Localization to Human Tumor Xenografts

Tumors were grown subcutaneously in immunocompromised mice (NCI-H358NSCLC in nu/nu mice and HT29 colon adenocarcinoma in SCID mice) untilthe tumor volume was approximately 1 cm³. 100 μg of unlabeled antibodyfor studies using SCID mice, or 100 μg of biotinylated antibody forstudies using nude mice, was injected intravenously via a tail vein.Twenty four hours later, the mice were anesthetized, perfused with PBS,and tumor and organs including heart, lungs, liver, kidneys, intestinesand spleen were collected and snap frozen in liquid nitrogen.

The tumor and organs from each mouse were sectioned on a cryostat andstained for antibody immunohistochemically as above, with the exceptionthat sections from the nude mice were developed using peroxidase labeledstreptavidin-biotin complex (Dako, Carpinteria, Calif.) and the sectionsfrom the SCID mice were developed using two peroxidase-conjugatedsecondary antibodies, a goat anti-mouse IgG +IgM followed by a rabbitanti-goat IgG.

B. Results

In Vivo Localization in Tumor-Bearng Mice

The in vivo localization of 2C3, 3E7, and GV39M in human tumorxenografts was determined. 100 μg of biotinylated 2C3 or isotype-matchedcontrol IgG were injected i.v. into nu/nu mice bearing NCI-H358 humanNSCLC. 100 μg of GV39M and 3E7 or isotype-matched control IgG wereinjected into SCID mice bearing HT29 human colonic adenocarcinomas.Twenty-four hours later, the mice were sacrificed, exsanguinated and thetumors and tissues were removed. Frozen sections of the tumors andtissues were analyzed immunohistochemically to determine the binding anddistribution of the antibodies (Table 4).

TABLE 4 TISSUE DISTRIBUTION OF ANTI-VEGF ANTIBODIES IN TUMOR BEARINGMICE Immunohistochemical Reactivity Antibody Heart Lung Liver Kidney¹Intestine Spleen Tumor² 2C3 − − − − − − 3+ 3E7 − − − − − − 1-2+ GV39M −− − 2+ − − 2+ Control³ − − − − − − Immunohistochemical analysis wasperformed on acetone fixed frozen sections of tissues, including thetumor, from tumor-bearing mice that had received 100 mg of the indicatedantibody intravenously 24 hours prior to sacrifice. The sections wereexamined microscopically and scored for specific reactivity as follows:−, negative; +/−, very weak; +, weak; 2+, moderate; 3+, strong; 4+, verystrong. ¹GV39M specifically bound endothelial or mesangial cells in theglomeruli of the kidney ²3E7 and GV39M specifically bound tumor vascularendothelium while 2C3 specifically bound tumor stroma. ³Contol = IgM ofirrelevant specificity

3E7 specifically localized to vascular endothelium within the tumors.Approximately 70% of MECA 32 positive blood vessels were stained by 3E7injected in vivo. The larger blood vessels that feed themicrovasculature were 3E7-positive. Small microvessels in both thetracks of stroma and in the tumor nests were also positive for 3E7. Theintensity of the staining by 3E7 was increased in and around areas offocal necrosis. In necrotic areas of the tumor, extravascular antibodywas evident, but in healthy regions of the tumor there was littleevidence of extravascular staining. Vascular endothelium in all normaltissues examined, including the kidney, was unstained by 3E7.

GV39M also specifically localized to vascular endothelium of the tumors.Approximately 80% of the MECA 32 positive blood vessels in the tumorwere stained by GV39M. The GV39M positive vessels were distributedevenly throughout the tumor, including large blood vessels, but alsosmall capillaries. As with 3E7, the staining intensity of the GV39Mpositive blood vessels was increased in areas of focal necrosis in thetumor. However, unlike 3E7, endothelial cells or mesangial cells in thekidney glomeruli were also stained. It appears that the staining of theglomeruli by GV39M is antigen-specific, since a control IgM ofirrelevant specificity produced no staining of the glomeruli. Vascularendothelium in tissues other than the kidney was not stained by GV39M.

Biotinylated 2C3 produced intense staining of connective tissuesurrounding the vasculature of the H358 human NSCLC tumor after i.v.injection. The large tracks of stromal tissue that connect the tumorcell nests were stained by 2C3, with the most intense localization beingobserved in the largest tracks of stroma. It was not possible todistinguish the vascular endothelium from the surrounding connectivetissue in these regions. However, the endothelial cells in vessels notsurrounded by stroma, such as in vessels running through the nests oftumor cells themselves, were stained. There was no detectable stainingby 2C3 in any of the normal tissues examined.

In the HT29 human tumor model, 2C3 also localized strongly to theconnective tissue but the most intense staining was observed in thenecrotic regions of the tumor.

EXAMPLE IV 2C3 Inhibits VEGF Binding to VEGFR2, but not VEGFR1

A. Materials and Methods

1. Cell Lines and Antibodies

Porcine aortic endothelial (PAE) cells transfected with either VEGFR1(PAE/FLT) or VEGFR2 (PAE/KDR) were obtained from Dr. JohannesWaltenberger (Ulm, Germany), prepared as described in Waltenberger etal. (1994, specifically incorporated herein by reference), and weregrown in F-12 medium containing 5% FCS, L-glutamine, penicillin, andstreptomycin (GPS). bEND.3 cells were obtained from Dr. Werner Risau(Bad Nauheim, Germany) and were grown in DMEM medium containing 5% FCSand GPS. NCI-H358 NSCLC (obtained from Dr. Adi Gazdar, UT-Southwestern,Dallas, Tex.), A673 human rhabdomyosarcoma, and HT1080 humanfibrosarcoma (both from American Type Culture Collection) were grown inDMEM medium containing 10% FCS and GPS.

2C3 and 3E7, anti-VEGF monoclonal antibodies, and 1A8, monoclonalanti-Flk-1 antibody, and T014, a polyclonal anti-Flk-1 antibody are asdescribed above in Example I and in Brekken et al. (1998) and Huang etal. (1998), each specifically incorporated herein by reference. A4.6.1,mouse anti-human VEGF monoclonal antibody, was obtained from Dr. Jin Kim(Genentech Inc., Calif.) and has been described previously (Kim et al.,1992; specifically incorporated herein by reference). Negative controlantibodies used were OX7, a mouse anti-rat Thyl1.1 antibody (Bukovsky etal., 1983), obtained from Dr. A. F. Williams (MRC Cellular ImmunologyUnit, Oxford, UK) and C44, a mouse anti-colchicine antibody (Rouan etal., 1990, obtained from ATCC).

2. ELISA Analysis

The extracellular domain of VEGFR1 (Flt-1/Fc, R&D Systems, Minneapolis)or VEGFR2 (sFlk-1-biotin) was coated directly on wells of a microtiterplate or captured by NeutrAvidin (Pierce, Rockford, Ill.) coated wells,respectively. VEGF at a concentration of 1 nM (40 ng/ml) was incubatedin the wells in the presence or absence of 100-1000 nM (15 μg-150 μg/ml)of control or test antibodies. The wells were then incubated with 1μg/ml of rabbit anti-VEGF antibody (A-20, Santa Cruz Biotechnology,Santa Cruz, Calif.).

The reactions were developed by the addition of peroxidase-labeled goatanti-rabbit antibody (Dako, Carpinteria, Calif.) and visualized byaddition of 3,3′5,5′-tetramethylbenzidine (TMB) substrate (Kirkegaardand Perry Laboratories, Inc.). Reactions were stopped after 15 min with1 M H₃PO₄ and read spectrophotometrically at 450 nM.

The assay was also performed by coating wells of a microtiter plate witheither control or test IgG. The wells were then incubated withVEGF:Flt-1/Fc or VEGF:sFlk-1-biotin and developed with eitherperoxidase-labeled goat anti-human Fc (Kirkegaard and PerryLaboratories, Inc.) or peroxidase-labeled streptavidin, respectively andvisualized as above.

3. Coprecipitation Assay

40 ng of VEGF was preincubated with the F(ab′)₂ of either of 2C3 (20 μg)or A4.6.1 (10 and 1 μg) for 30 min in binding buffer (DMEM with 1 mMCaCl₂, 0.1 mM CuSO₄, and 0.5% tryptone). 200 ng of soluble forms ofVEGFR1 (Flt-1/Fc) or VEGFR2 (KDR/Fc. R&D Systems, Minneapolis, Minn.)were added for a total volume of 50 μl and incubated for 2 hrs. Thereceptor/Fc constructs were precipitated using Protein A-sepharose beadsand the resulting precipitate was washed 4 times with binding buffer.

Reducing sample buffer was added to the pellet and supernatant of eachreaction and both were analyzed by 12% SDS-PAGE and transferred to PVDFmembranes. The membranes were then probed with 12D7 (1.0 μg/ml), a mouseanti-VEGF antibody and developed after incubation withperoxidase-labeled goat anti-mouse IgG (Kirkegaard & Perry Laboratories,Inc.) by Super Signal chemiluminescence substrate (Pierce, Rockford,Ill.). The soluble receptor/Fc constructs were also detected by usingperoxidase-conjugated goat anti-human Fc (Kirkegaard & PerryLaboratories, Inc.)

B. Results

1. 2C3 blocks VEGF Binding to VEGFR2 but not to VEGFR1 in ELISAs

The anti-VEGF antibody 2C3 blocked VEGF from binding to VEGFR2(KDR/Flk-1) but not to VEGFR1 (FLT-1) in the ELISA assay. In thepresence of a 100-fold and 1000-fold molar excess of 2C3, the amountVEGF that bound to VEGFR2-coated wells was reduced to 26% and 19%,respectively, of the amount that bound in the absence of 2C3 (FIG. 2).In contrast, in the presence of a 100-fold and 1000-fold molar excess of2C3, the amount VEGF that bound to VEGFR1-coated wells was 92% and 105%,respectively, of the amount that bound in the absence of 2C3 (FIG. 2).

The amounts of VEGF that bound to VEGFR1 or VEGFR2 were unaffected bythe presence of a 100-1000 fold excess of the non-blocking monoclonalanti-VEGF antibody 3E7 or of a control IgG of irrelevant specificity(FIG. 2). A4.6.1 blocked VEGF binding to both VEGFR2 (KDR/Flk-1) andVEGFR1 (FLT-1).

2. 2C3 Blocks VEGF Binding to VEGFR2 but not to VEGFR1 in Solution

The ability of 2C3 to block the binding of VEGF to VEGFR1/Fc orVEGFR2/Fc in solution was assessed in co-precipitation assays. 40 ng ofVEGF was incubated with 200 ng extracellular domain of VEGFR1 linked toan Fc portion (Flt-1/Fc) or VEGFR2 (KDR/Fc) linked to an in the presenceor absence of 2C3 or 4.6.1 F(ab′)₂. The receptor/Fc constructs wereprecipitated by incubation with Protein A sepharose beads. Theprecipitate was washed and resuspended in reducing sample buffer andseparated by 12% SDS-PAGE and transferred to PVDF. The membrane wasblocked with PP82 and probed with 12D7 (1 μg/ml) mouse anti-VEGFantibody and developed under standard chemiluminescence conditions. VEGFmonomer and dimer along with F(ab′)₂ were detected.

VEGF mixed with either VEGFR1/Fc or VEGFR2/Fc was co-precipitated byProtein A sepharose, showing that VEGF binds to both receptors. Additionof 2C3 F(ab′)₂ blocked the binding of VEGF to VEGFR2/Fc, but not toVEGFR1/Fc. In contrast, 4.6.1 F(ab′)₂ blocked the binding of VEGF toboth VEGFR2/Fc and VEGFR1/Fc. The results affirm that 2C3 inhibits thebinding of VEGF to VEGFR2 but not to VEGFR1, whereas the 4.6.1 antibodyinhibits the binding of VEGF to both VEGFR2 and VEGFR1.

EXAMPLE V 2C3 Blocks VEGF-Induced Phosphorylation of VEGFR2

A. Materials and Methods

Immunoprecipitation and Western Blot Analysis

PAE/KDR, PAE/FLT, and bEND.3 cells were grown to 80-90% confluency in100 mm tissue dishes in media containing 5% serum. The cells were thenserum starved for 24 hours in media containing 0.1% serum. Afterpretreatment with 100 nM sodium orthovanadate in PBS for 30 min, thecells were incubated with 5 nM (200 ng/ml) VEGF165, 5 nM (100 ng/ml)bFGF (R&D Systems, Minneapolis, Minn.), or A673 tumor conditioned mediain the presence or absence of control or test antibodies for additional15 min.

The cells were then washed with ice-cold PBS containing 10 mM EDTA, 2 mMsodium fluoride, and 2 mM sodium orthovanadate and lysed in lysis buffer(50 mM Tris, 150 mM NaCl, 1% Nonidet P-40, 0.25% sodium deoxycholate,0.1% CHAPS, 5 mM EDTA, 1.5 mM MgCl2, 2 mM sodium fluoride, 2 mM sodiumorthovanadate, 10% glycerol and protease inhibitors (Complete ProteaseInhibitor Cocktail tablets, Boehringer Mannheim)). The lysates wereclarified by centrifugation and resulting supernatant used forimmunoprecipitation

VEGFR1 and VEGFR2 were immunoprecipitated by incubating the cell lysatesovernight at 4° C. with 5 μg of chicken anti-FLT-1 N-terminus (UpstateBiotechnology, Lake Placid, NY) or 10 μg of T014 (affinity purifiedanti-Flk-1), respectively. The reactions using the chicken anti-FLT-1antibody were subsequently incubated with a bridging goat anti-chickenantibody (Kirkegaard and Perry Laboratories, Inc.) for 1 h at 4° C. Theimmune complex was then precipitated with Protein A/G sepharose, washedmultiple times with 10% lysis buffer (with added protease inhibitors) inPBS-tween (0.2%) and boiled in SDS sample buffer containing 100 mMβ-mercaptoethanol and 8 M urea.

The samples were then separated by SDS-PAGE and transferred to PVDFmembranes. The membranes were blocked for 30-60 min with PP81 (EastCoast Biologics, Berwick, Me.) and probed for phosphotyrosine residueswith 0.5 μg/ml of 4G10 (Upstate Biotechnology, Lake Placid, N.Y.)overnight at 4° C. The PVDF membranes were developed after incubationwith peroxidase-labeled rabbit anti-mouse IgG (Dako, Carpinteria,Calif.) by Super Signal chemiluminescence substrate (Pierce, Rockford,Ill.). The PVDF membranes were then stripped with ImmunoPure Elutionbuffer (Pierce, Rockford, Ill.) for 30 min at 55° C. and reprobed forreceptor levels with either 0.5 μg/ml chicken anti-FLT-1 or 1.0 μg/mlT014 and developed as above after incubation with the appropriateperoxidase-conjugated secondary antibody.

B. Results

Blocking of VEGF4Induced Phosphorylation

In these studies, PAE/KDR cells were stimulated for 15 min. with PBS,bFGF (5 nM, 100 ng/ml), VEGF165 (5 nM, 210 ng/ml), A673 conditionedmedia (CM), CM in combination with particular antibodies (CNTL, 2C3,3E7, A4.6.1 separately at 100 nM, 15 μg/ml), or T014 alone (100 nM, 15μg/ml). PAE/FLT cells were also stimulated for 15 min. with PBS, VEGF165(5 nM, 210 ng/ml), A673 conditioned media (CM), CM in combination withparticular antibodies (2C3, 3E7, A4.6.1 separately at 100 nM, 15 μg/ml),or T014 alone (100 nM, 15 μg/ml). The cells were then incubated in lysisbuffer and the receptor was immunoprecipitated, separated by SDS-PAGEunder reducing conditions, transferred to PVDF membranes and probed with4G10 (0.5 μg/ml), mouse anti-phospho-tyrosine antibody, and developedunder standard chemiluminescence conditions. The membranes were thenstripped and re-probed with the immunoprecipitating IgG to determine thelevel of receptor protein in each lane.

The results showed that 2C3, along with A4.6.1, a control neutralizinganti-VEGF antibody, block VEGF-induced phosphorylation of VEGFR2 inPAE/KDR cells. This is in agreement with previous results thatdemonstrated both 2C3 and A4.6.1 block VEGF-mediated growth ofendothelial cells (Example II; Brekken et al., 1998). Western blots ofVEGFR2 in the immunoprecipitates were conducted to demonstrate theamounts of VEGFR2 protein in each lane. 3E7, which sees an NH₂-terminalepitope of VEGF, did not block VEGF-induced phosphorylation of VEGFR2nor did a control IgG of irrelevant specificity.

The effect of 2C3 on VEGF-induced phosphorylation of VEGFR1 is notclear. As other investigators have shown, VEGF-induced phosphorylationof VEGFR1 in PAE/FLT cells is difficult to demonstrate, possibly due tothe low intrinsic kinase activity of VEGFR1 (De Vries et al., 1992;Waltenberger et al., 1994; Davis-Smyth et al., 1996; Landgren et al.,1998).

EXAMPLE VI 2C3 Inhibits VEGF-Induced Permeability

A. Materials and Methods

Miles Permeability Assay

The protocol followed was as described by Murohara, et al. (1998;specifically incorporated herein by reference). Briefly, 400-450 g,male, IAF hairless guinea pigs (Charles River, Wilmington, Mass.) wereanesthetized and then injected i.v. with 0.5 ml of 0.5% Evan's blue dyein sterile PBS through an ear vein. Twenty min later 20 ng of VEGF inthe presence or absence of control or test antibodies was injectedintradermally (i.d.). The resultant blue spots in the back of the guineapig were photographed and measured with a caliper 30 min after the i.d.injections.

B. Results

2C3 Blocks VEGF-Induced Permeability

To investigate the effects of 2C3 on VEGF-induced permeability, IAFhairless guinea pigs (Hartley strain) 400-450 g in size wereanesthetized and injected i.v. with 0.5 ml of 0.5% Evan's blue dye insterile PBS through an ear vein. Twenty minutes later, 25 ng of VEGF inthe presence or absence of control or test antibodies was injectedintradermally (i.d.). The resultant blue spots in the back of the guineapig were photographed and measured with a caliper 30 minutes after thei.d. injections.

Using this Miles permeability assay, it was found that 2C3, which blocksVEGF from =activating VEGFR2, inhibited VEGF-induced permeability in theguinea pigs. This effect was evident with 2C3 at a 10-fold, 100-fold, or1000-fold molar excess over VEGF. A4.6. 1, which blocks VEGF fromactivating both VEGFR1 and VEGFR2, blocked VEGF-induced permeability at10-fold molar excess (present studies and Kim et al., 1992). 3E7, and acontrol IgG that do not block VEGF:VEGFR2 interaction also do not blockVEGF-induced permeability in the Miles permeability assay in guineapigs.

These results suggest endothelial permeability mediated by VEGF ismediated, at least in part, through VEGFR2 activation. These resultsaccord with those of other investigators who have shown that thetyrosine kinase activity of VEGFR2 is necessary for VEGF-inducedpermeability (Murohara et al, 1998; Joukov et al., 1998; Ogawa et al.,1998).

EXAMPLE VII Anti-Tumor Effects of 2C3

A. Materials and Methods

1. In Vivo Tumor Growth Inhibition

Nu/nu mice were injected subcutaneously with either 1×10⁷ NCI-H358 NSCLCcells or 5×10⁶ A673 rhabdomyosarcoma cells on day 0. On day 1 andsubsequently twice per wk the mice were given i.p. injections of 2C3 at1, 10, or 100 μg or controls as indicated The tumors were then measuredtwice per wk for a period of approximately six wk for the NCI-H358bearing mice and four wk for the A673 bearing mice. Tumor volume wascalculated according to the formula: volume=L×W×H, where L=length,W=width, H=height.

2. In Vivo Tumor Therapy

Male nu/nu mice bearing subcutaneous NCI-H358 tumors or HT1080fibrosarcoma 200-400 mm³ in size were injected i.p. with test or controlantibodies. The NCI-H358 bearing mice were treated with 100 μg ofantibodies per injection three times a week during the first week andtwice a week during the second and third week. The mice were thenswitched to 50 μg per injection every five days. The HT1080 bearing micewere treated with 100 μg of the indicated antibody or saline every otherday throughout the duration of the study. In both studies, mice weresacrificed when their tumors reached 2500 mm³ in size or earlier iftumors began to ulcerate.

B. Results

1. 2C3 Growth Inhibition of Newly-Implanted Human Tumor Xenografts

2C3 inhibits the in vivo growth of both NCI-H358 NSCLC and A673rhabdomyosarcoma in nu/nu mice in a dose dependent manner (FIG. 3A andFIG. 3B). 100 μg of 2C3 given i.p. 2 times per wk to mice that had beeninjected with tumor cells subcutaneously one day earlier inhibited thegrowth of both human tumor types. The final tumor volume in the 2C3recipients was approximately 150 mm³ in both tumor systems, as comparedwith approximately 1000 mm³ in the recipients of controls.

Treatment with either 10 or 1 μg of 2C3 twice per wk was less effectiveat preventing tumor growth. However, both lower doses of 2C3 did slowthe growth of A673 tumors to a similar degree compared to the untreatedmice. The tumor growth retardation caused by a 10 μg dose of 2C3 wasless marked in the NCI-H358 tumor model. The differences between thesetwo tumor models and their response to inhibition of VEGFR2 activity by2C3 correlates with the aggressiveness of the two types of tumors invivo. NCI-H358 grows in vivo much more slowly than does A673 and appearsto be less sensitive to low doses of 2C3, whereas, A673 tumors grow morequickly and aggressively and appear to be more sensitive to lower dosesof 2C3.

3E7, which binds to VEGF but does not block its activity, had no effecton the growth of NCI-H358 tumors. However, 3E7 given at a dose of 100 μgtwice per wk stimulated the growth of A673 tumors (FIG. 3B), suggestingthat it increases the efficiency of VEGF signaling in the tumor.

2. Treatment of Established Human Tumor Xenografts with 2C3

Mice bearing subcutaneous NCI-H358 NSCLC tumors that had grown to a sizeof approximately 300-450 mm3 were injected i.p. with 2C3, A4.6.1, 3E7,or an IgG of irrelevant specificity (FIG. 4). Doses were 50-100 μg every3-5 days. A4.6.1 was used as a positive control because it has beenshown by other investigators to block VEGF activity in vivo resulting inan inhibition of tumor growth (Kim et al., 1993; Mesiano et al., 1998).In addition to measuring mean tumor volume (FIG. 4), photographs of themice from each treatment group were also taken to show the differencesin tumor size and appearance at the end of the study.

Treatment with either 2C3 or A4.6.1 led to a slow regression of thetumors over the course of the study. The mean tumor volumes at the endof the study were 30% (2C3) and 35% (4.6.1) of the initial mean tumorvolume (FIG. 4). However, these results are complicated by the fact thatspontaneous retardation in tumor growth was observed in the controlgroups of mice between 40 days and 60 days after tumor cell injection.The results up to 40 days, before the spontaneous retardation in growthwas evident, show that treatment with 2C3 and A4.6.1 prevents tumorgrowth.

FIG. 5A shows a further study in which mice bearing NCI H358 weretreated for a prolonged period with 100 μg of either 2C3 or 3E7. In thisstudy, spontaneous regressions were less pronounced. The mean tumorvolume of the 2C3 treated mice at the start of treatment was 480 mm³ andafter approximately 14 wk of treatment the mean tumor volume dropped to84 mm³, a decrease of approximately 80% in volume. The 3E7 treated micebegan treatment with a mean tumor volume of 428 mm³ and rose to a volumeof 1326 mM³ after approximately 14 wk, an increase of 300% in volume.

FIG. 5B shows the tumor growth curves of mice bearing a humanfibrosarcoma, HT1080, that were every treated every two days with 100 pgof 2C3, 3E7, or a control IgG, or saline. 2C3 arrested the growth of thetumors for as long as treatment was continued. The mice treated with3E7, control IgG, or saline bore tumors that grew progressively and to asize that required the mice to be sacrificed less than 4 weeks aftertumor cell injection.

EXAMPLE VIII 2C3 is Distinct from A4.6.1

There are a number differences between 2C3 and A4.6.1 (e.g., Table 5).The antibodies recognize distinct epitopes on VEGF based upon ELISAcross-blocking studies (Example I). Mutagenesis and X-raycrystallographic studies have earlier shown that A4.6.1 binds to anepitope on VEGF that is centered around amino acids 89-94 (Muller etal., 1998).

Of particular interest is the fact that A4.6.1 blocks VEGF from bindingto both VEGFR1 and VEGFR2 (Kim et al., 1992; Wiesmann et al., 1997;Muller et al.,1998; Keyt et al., 1996), while 2C3 only blocks VEGF frombinding to VEGFR2 (Example IV). Compelling published evidence thatA4.6.1 inhibits VEGF binding to VEGFR2 and VEGFR1 comes from detailedcrystallographic and structural studies (Kim et al., 1992; Wiesmann etal, 1997; Muller et al. ,1998; Keyt et al., 1996; each incorporatedherein by reference). The published data indicate that A4.6.1 inhibitsVEGF binding to VEGFR2 by competing for the epitope on VEGF that iscritical for binding to VEGFR2, and blocks binding of VEGF to VEGFR1most probably by steric hindrance (Muller et al. ,1998; Keyt et al.,1996).

A humanized version of A4.6.1 is currently in clinical trials (Brem,1998; Baca et al., 1997; Presta et al., 1997; each incorporated hereinby reference). Macrophage/monocyte chemotaxis and other endogenousfunctions of VEGF that are mediated through VEGFR1 will most likely beimpaired in the A4.6.1 trials. In contrast, 2C3 is envisioned to besuperior due its ability to specifically block VEGFR2-mediated effects.2C3 is thus potentially a safer antibody, particularly for long-termadministration to humans. The benefits of treatment with 2C3 include theability of the host to mount a greater anti-tumor response, by allowingmacrophage migration to the tumor at the same time it is blockingVEGF-induced tumor vasculature expansion. Also, the many systemicbenefits of maintaining macrophage chemotaxis and other effects mediatedby VEGFR1 should not overlooked.

TABLE 5 CHARACTERISTICS OF THE ANTI-VEGF ANTIBODIES 2C3 AND A4.6.1Characteristic 2C3 A4.6.1 Isotype IgG2a, k IgG1¹ Epitope on VEGFUndefined, but distinct Continuous, from A4.6.1² centered around aminoacids 89-94 Affinity 1 × 10⁻⁹ (M)³ 8 × 10⁻¹⁰ (M) Blocks VEGF frombinding No Yes to VEGFR1 Blocks VEGF from binding Yes Yes to VEGFR2Blocks VEGF-induced Yes Yes permeability Blocks VEGF-induced Yes Yesproliferation Direct IHC pattern on NR Weak reactivity frozen tumorsections with some BV⁴ In vivo tumor localization Moderate to strongModerate reactivity pattern reactivity with CT with a minority of BV,weak to no reactivity with CT In vivo normal mouse None detectable Nonedetectable tissue localization Abbreviations used: IHC,immunohistochemistry; NR, no reactivity; BV, blood vessels: CT,connective tissue. ¹References for A4.6.1 data include Kim et al., 1992;Wiesmann et al., 1997; Muller et al., 1998; and Keyt et al., 1996, eachincorporated herein by reference ²The epitope that 2C3 recognizes onVEGF is undefined but has been shown to be distinct from the epitopethat A4.6.1 recognizes through ELISA cross-blocking studies ³Theaffinity of 2C3 for VEGF has been estimated by ELISA and surface plasmonresonance analysis. ⁴A4.6.1 only reacts with lightly fixed acetone fixedfrozen sections.

EXAMPLE IX VEGF Staining in Arthritic Tissue

The relationship between angiogenesis and disease extends beyond thatobserved in vascularized tumors. For example, the involvement ofaberrant angiogenesis is well documented in arthritis. A panel ofdifferent anti-VEGF antibodies and antibodies to thymidine phosphorylasehave been used to stain arthritic tissue and differentiate this frommatched controls. Studies using antibodies against VEGF have shownstriking expression in the pannus of rheumatoid arthritis.

EXAMPLE X 2C3-Endostatin Conjugates

A. Cloning and Expression of Endostatin

RNA was isolated from mouse liver and used as the template for RT-PCR™with the following primers:

5′ primer aga cca tgg gtc ata ctc atc agg act ttc a (SEQ ID NO:43);

3′ primer ctac cat ggc tat ttg gag aaa gag gtc a (SEQ ID NO:44).

The resultant cDNA fragment has the DNA sequence of SEQ ID NO:12 and theamino acid sequence of SEQ ID NO: 13. For reference, the humanendostatin amino acid sequence is SEQ ID NO:14. The mouse cDNA fragmentwas cloned into the expression vector H6pQE60 (Qiagen), which encodes anN-terminal 6× histidine tag, and then expressed in E. coli Ml5 cells.When E. coli cell density reached an optical density of 0.6 at 560 nM,0.1 mM isopropylthiogalactoside (IPTG) was added for 4 hours to induceexpression of 6-His endostatin. The cells were harvested bycentrifugation and lysed in lysis buffer (B-PER Bacterial ProteinExtraction Reagent (Pierce, Rockford, Ill.)).

The inclusion bodies, which contained the 6-His endostatin, weresedimented by centrifugation and dissolved in buffer A (pH 8.0, 6 Mguanidine HCI (GuHCL), 100 mM NaH₂PO₄, 10 mM Tris, 10 mM imidazol, 10 mMβ-2 mercaptoethanol). The solution containing the reduced 6-Hisendostatin was treated with an excess of5,5′-dithio-bis-(2-nitrobenzoic) acid (Ellman's reagent) (20 mM) andloaded onto a Ni-NTA column. The column was washed with wash buffer (6 MGuHCl, 100 mM NaH₂PO₄, 10 mM Tris, 500 mM NaCl, pH 7.3) and 6-Hisendostatin was eluted from the column with 0.2 M imidazole in washbuffer.

The eluted and insoluble 6-His endostatin was diluted with an equalvolume of refolding buffer (3M urea, 1M Tris pH 7.3, 0.5 M L-arginine,0.5 M NaCl, 0.1 M Na₂HPO₄, 1 mM reduced glutathione (GSH)) and incubatedovernight at room temperature. Refolded 6-His endostatin was dialyzedextensively against PBS, pH 7.4 at room temperature. The resultingprotein, 6-His endostatin was soluble and highly pure based uponSDS-PAGE analysis under non-reducing conditions where it ran as a single20 kDa band.

B. Functional Activity of Endostatin

In addition to the fact that the expressed protein is fully soluble,other evidence that E. coli expressed 6-His endostatin is biologicallyactive includes demonstrated binding to endothelial cells. Biotinylated6-His endostatin was prepared and incubated with three differentendothelial cell types in vitro (Bend3 mouse endothelial cells; ABAE,bovine aortic endothelial cells; and HUVEC, human umbilical veinendothelial cells). Binding was detected using streptavidin-peroxidasein conjunction with O-phenylenediamine (OPD) and the absorbance read at490 nm.

The direct binding studies showed that (Biotinylated 6-His) endostatinbound in a saturable fashion to these three different types ofendothelial cells in vitro. Also, expressed endostatin (without label)was shown to compete with biotinylated endostatin for binding to Bend3endothelial cells.

C. Conjugation of Endostatin to 2C3 via SMPT and 24T

4-Succinimidyloxycarbonyl-α-methyl-α-(2-pyridyldithio)-toluene (SMPT) inN′N-dimethylformamide (DMF) was added to 2C3 IgG at a molar ratio of 5:1(SMPT:2C3) and incubated at room temperature (RT) for 1 hr in PBS with 5mM EDTA (PBSE). Free SMPT was removed by G25 size exclusionchromatography run in PBSE. Concurrently, mouse 6-His endostatin wasincubated with 2-iminothiolane (2-IT, Traut's reagent) at a molar ratioof 1:5 (endostatin:2-IT) for 1 hour at RT. Free 2-IT was removed by G25size exclusion chromatography run in PBSE.

SMPT-modified 2C3 was mixed with 2-IT-modified 6-His endostatin,concentrated to 3-5 ml, and incubated for 24 h at RT with gentleshaking. The reaction was analyzed by SDS-PAGE. Unconjugated 2C3-SMPTwas removed from the conjugate by heparin affinity chromatography, thusproviding 2C3-endostatin.

D. Conjugation of Endostatin to 2C3 via SMCC and SATA

N-Succinimidyl S-acetylthioacetate (SATA) was incubated with6-His-endostatin at a molar ratio of 6:1 (SATA:endostatin) for 30 min atRT. Free SATA was removed by G25 size exclusion chromatography run inPBSE. SATA modified 6-His endostatin in PBSE was concentrated to 4.0 mland 0.4 ml deacetylation solution (0.1 M hydroxylamine) was added. Themixture was incubated at RT for 2 hr. Concurrently, 2C3 IgG, in PBSE,was incubated with succinimidyl4-(N-maleimidomethyl)cyclohexane-1-carboxylate (SMCC) at a molar ratioof 1:5 (2C3: SMCC). Free SMCC was removed by G25 size exclusionchromatography run in PBSE.

Deacetylated SATA modified endostatin was then incubated with SMCCmodified 2C3, concentrated to approximately 5 mg/ml total protein undernitrogen, and incubated overnight at RT with gentle stirring. Thereaction was analyzed by SDS-PAGE. Unconjugated 2C3-MCC was removed fromthe 2C3-endostatin conjugate by heparin affinity chromatography in PBSE,thus providing 2C3-endostatin. Successful conjugation was also achievedusing 2-iminothiolane rather than SATA as the thiolating agent.

E. Fusion Proteins of 2C3 and Endostatin

As the DNA sequences for mouse and human endostatin, and for 2C3 areavailable (and provided herein), 2C3-endostatin fusion proteins canreadily be prepared. The expression and refolding of endostatin, asdescribed above, shows that successful recombinant expression of thismolecule is indeed possible.

The preparation of a 2C3-endostatin fusion protein can be in a formwhere endostatin is present at the C-terminus of a 2C3 heavy chain or islinked to a 2C3 ScFv fragment. In these cases, recombinant technologymakes it straightforward to vary the linkage, and the use of selectivelycleavable sequences to join the two functional portions is particularlyenvisioned. Plasmin-cleavable or MMP-cleavable sequences are currentlypreferred.

The availability of selectively cleavable sequences and adaptability ofrecombinant technology also provides for 2C3-endostatin fusion proteinsin which the endostatin is substituted at another point of the 2C3construct. The endostatin will remain embedded within 2C3 until contactwith an enzyme that acts on the selectively cleavable sequence, at whichpoint functional endostatin is released from the fusion protein.

EXAMPLE XI 2C3-Ang-2 Conjugates

A. Expression of Ang-2

To construct a 2C3-Ang-2 conjugate, Ang-2 is preferably used inrecombinant form, as may be produced in insect cells using a baculovirusexpression system. The currently preferred protocol for Ang-2 expressionand purification involves cloning Ang-2 cDNA from mouse placenta RNA byRT-PCR™ and cloning the Ang-2 cDNA into pFastBac1 expression vector.Competent DH10Bac E. coli cells are transformed with the recombinantplasmid.

After antibiotic selection, E. coli colonies containing recombinantBacmid are picked, grown and recombinant Bacmid DNA purified. Insectcells SF9 are transfected with the recombinant Bacmid DNA using theCellfectin reagent. Recombinant baculovirus are harvested from thesupernatant of the transfected SF9 cells. Recombinant baculovirus areamplified and used to infect SF9 cells and the infected SF9 cells willexpress Ang-2. Ang-2 is purified from the supernatant of such infectedSF9 cells by affinity purification.

B. Conjugation of Ang-2 to 2C3

Purified 2C3 is conjugated to recombinant Ang-2 using the chemicallinker SMPT, generally as described above. SMPT in N′N-dimethylformamide(DMF) is added to 2C3 IgG at a molar ratio of 5:1 (SMPT:2C3) andincubated at room temperature (RT) for 1 hr in PBS with 5 mM EDTA(PBSE). Free SMPT is removed by G25 size exclusion chromatography run inPBSE. Concurrently, recombinant Ang-2 is incubated with 2-IT at RT. Free2-IT is removed by G25 size exclusion chromatography run in PBSE.

SMPT-modified 2C3 is mixed with 2-IT-modified recombinant Ang-2,concentrated, and incubated for 24 h at RT with gentle shaking. Thereaction is analyzed by SDS-PAGE. Unconjugated 2C3-SMPT is removed fromthe conjugate by gel filtration chromatography, thus providing2C3-endostatin.

EXAMPLE XII 2C3-Tissue Factor Conjugates

2C3 was modified with SMPT, as described in the foregoing examples. FreeSMPT was removed by G25 chromatography as outlined above except that thepeak (2C3-SMPT) was collected under nitrogen. 600 μl of 2C3-SMPT wasremoved to quantitate thiopyridyl groups after addition ofdithiothreitol (DTT) to 50 mM. An average of 3 MPT groups wereintroduced per IgG. Human truncated tissue factor (tTF) having acysteine residue introduced at the N-terminus was reduced with 5 mM ,2-ME. , 2-ME was removed by G25 chromatography.

Reduced N-Cys-tTF was pooled with the 2C3-SMPT and incubated at a molarratio of 2.5:1 (tTF:IgG) for 24 hours at RT. The reaction wasconcentrated to 1-2 ml using an Amicon with a 50,000 molecular weightcut off (MWCO) membrane. Unconjugated tTF and IgG were separated fromconjugates using Superdex 200 size exclusion chromatography, thusproviding 2C3-tTF.

EXAMPLE XIII 2C3-CRM107 Conjugates

2C3 was modified with SMPT. The cytotoxic agent, CRM107 (from Dr. JerryFulton, Inland Laboratories, DeSoto, Tex.), was modified with 2-IT asdescribed in the foregoing examples. SMPT modified 2C3 was incubatedwith 2-IT modified CRM107 at a molar ratio of 1:5 (IgG:CRM107) for 24 hrat RT with gentle shaking. Conjugated 2C3 was separated from freereactants by superdex 200 size exclusion chromatography thus providing2C3-CRM 107.

EXAMPLE XIV 2C3 ProDrug Studies

A. Cloning and Expression of β-glucuronidase (GUS)

A plasmid (pBacgus-1) containing the E. coli GUS gene was obtained fromNovagen, Inc. The plasmid was used a template for PCR to clone the GUSgene into the H6pQE60 expression vector, which encodes an N-terminal6×histidine tag. E. coli Ml5 cells carrying the plasmid were grown tountil the cell density reached an optical density of 0.6 at 560 nM. 0.1mM isopropylthiogalactoside (IPTG) was added to induce expression of 6his GUS. After 4 hours, the cells were harvested by centrifugation.

The E. coli pellet as lysed in cell lysis buffer (B-PER BacterialProtein Extraction Reagent (Pierce, Rockford, Ill.)). The solution wasloaded onto a Ni-NTA column, the column washed with wash buffer (6 MGuHCl, 100 mM NaH₂PO₄, 10 mM Tris, 500 mM NaCl, pH 7.3) and the bound6-His GUS was eluted with 0.2 M imidazole in the same buffer.

The 6-His GUS was pure based upon SDS-PAGE, where it ran as a singleband of 75 kDa band. On gel filtration columns, the 6-His GUS runs as atetramer of about 300 kDa. The 6-His GUS was enzymatically active asjudged by its ability to cleave the substratep-nitrophenyl-β-D-glucuronide (PNPG).

B. Conjugation of 2C3 to β-glucuronidase (GUS)

N-Succinimidyl S-acetylthioacetate (SATA) was incubated with GUS at amolar ratio of 6:1 (SATA:GUS) for 30 min at RT. Free SATA was removed byG25 size exclusion chromatography run in PBSE. SATA modified GUS in PBSEwas concentrated to 4.0 ml and 0.4 ml deacetylation solution (0.1 Mhydroxylamine) was added. The mixture was incubated at RT for 2 hr.Concurrently 2C3 IgG, in PBSE, was incubated with succinimidyl4-(N-maleimidomethyl)cyclohexane-1-carboxylate (SMCC) at a molar ratioof 1:5 (2C3: SMCC). Free SMCC was removed by G25 size exclusionchromatography run in PBSE.

Deacetylated SATA modified GUS was then incubated with SMCC modified 2C3overnight at RT with gentle stirring. Free GUS was removed byion-exchange chromatography on Q-Sepharose, with the free 2C3 and the2C3-GUS conjugate being eluted with 0.5 M NaCl in PBS. The resultantsolution was separated by Superdex 200 size exclusion chromatographyyielding 2C3-GUS with a purity of 90%.

C. Biological Activity of 2C3-GUS Conjugate

The biological activity of each component of the 2C3-GUS conjugate wasconfirmed. 2C3-GUS bound specifically to VEGF coated wells in anappropriately controlled ELISA, as detected by a secondary HRP-labelledanti-mouse IgG and OPD. Half maximal binding was observed at 0.1 nM.Thus, the 2C3 binding portion functions correctly. The GUS portion alsoretained enzymatic activity.

2C3-GUS was radioiodinated with ¹²⁵I to a specific activity of 5×10⁶cpm/μg After intravenous injection into mice, the radioiodinated 2C3-GUScleared from the blood with a t½α of about 6 hours and a t½ of about 25hours.

D. GUS Cleavable Prodrugs

β-glucuronide prodrugs, such as doxorubicin-β-glucuronide andcalcimycin-β-glucuronide were prepared essentially as described in U.S.Pat. No. 5,561,119, specifically incorporated herein by reference. Suchprodrugs are designed to release the cytotoxic component, such asdoxorubicin or calcimycin, only when degraded by a glycoside enzyme,such as GUS. By attaching GUS to 2C3, GUS is targeted specifically tothe tumor vasculature and stroma, thus providing for specific cleavageof the prodrugs and release of the cytotoxic component specificallywithin the tumor site.

E. Biological Activity of 2C3-GUS Conjugate

2C3-GUS specifically localized to tumor vasculature and surroundingtumor stroma after i.v. injection into SCID mice bearing human NCI-H358NSCLC tumors in the subcutaneous site. Presence of 2C3-GUS was detectedimmunohistochemically on frozen sections of tumors with HRP-labeledanti-mouse IgG or with HRP-labeled anti-GUS. Maximal localization wasobserved 24-48 hours after injection of 2C3-GUS. Normal tissues wereunstained. Specific localization of 2C3-GUS to tumor vasculature andsurrounding tumor stroma allows for a systemically administered prodrug,such as doxorubicin glucuronide or calcimycin- glucuronide, to beactivated only within the tumor.

A hybridoma cell line as described herein has been deposited under theprovisions of the Budapest Treaty with the American Type CultureCollection (ATCC), Manassas, Va., USA; and been assigned accessionnumber ATCC No. PTA 1595. The invention described and claimed herein isnot limited in scope by the PTA 1595 cell line deposited since thedeposited embodiment is an illustration of one aspect of the inventionand any equivalent hybridoma cell lines that produce functionallyequivalent monoclonal antibodies are within the scope of this invention.Indeed, all of the compositions and methods disclosed and claimed hereincan be made and executed without undue experimentation in light of thepresent disclosure.

While the compositions and methods of this invention have been describedin terms of preferred embodiments, it will be apparent to those of skillin the art that variations may be applied to the composition, methodsand in the steps or in the sequence of steps of the methods describedherein without departing from the concept, spirit and scope of theinvention. More specifically, it will be apparent that certain agentsthat are both chemically and physiologically related may be substitutedfor the agents described herein while the same or similar results wouldbe achieved. All such similar substitutes and modifications apparent tothose skilled in the art are deemed to be within the spirit, scope andconcept of the invention as defined by the appended claims.

REFERENCES

The following references, to the extent that they provide exemplaryprocedural or other details supplementary to those set forth herein, arespecifically incorporated herein by reference.

Abrams and Oldham, In: Monoclonal Antibody Therapy of Human Cancer, Foonand Morgan (Eds.), Martinus Nijhoff Publishing, Boston, pp. 103-120,1985.

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44 1 2149 DNA Homo sapiens 1 cagctgactc aggcaggctc catgctgaac ggtcacacagagaggaaaca ataaatctca 60 gctactatgc aataaatatc tcaagtttta acgaagaaaaacatcattgc agtgaaataa 120 aaaattttaa aattttagaa caaagctaac aaatggctagttttctatga ttcttcttca 180 aacgctttct ttgaggggga aagagtcaaa caaacaagcagttttacctg aaataaagaa 240 ctagttttag aggtcagaag aaaggagcaa gttttgcgagaggcacggaa ggagtgtgct 300 ggcagtacaa tgacagtttt cctttccttt gctttcctcgctgccattct gactcacata 360 gggtgcagca atcagcgccg aagtccagaa aacagtgggagaagatataa ccggattcaa 420 catgggcaat gtgcctacac tttcattctt ccagaacacgatggcaactg tcgtgagagt 480 acgacagacc agtacaacac aaacgctctg cagagagatgctccacacgt ggaaccggat 540 ttctcttccc agaaacttca acatctggaa catgtgatggaaaattatac tcagtggctg 600 caaaaacttg agaattacat tgtggaaaac atgaagtcggagatggccca gatacagcag 660 aatgcagttc agaaccacac ggctaccatg ctggagataggaaccagcct cctctctcag 720 actgcagagc agaccagaaa gctgacagat gttgagacccaggtactaaa tcaaacttct 780 cgacttgaga tacagctgct ggagaattca ttatccacctacaagctaga gaagcaactt 840 cttcaacaga caaatgaaat cttgaagatc catgaaaaaaacagtttatt agaacataaa 900 atcttagaaa tggaaggaaa acacaaggaa gagttggacaccttaaagga agagaaagag 960 aaccttcaag gcttggttac tcgtcaaaca tatataatccaggagctgga aaagcaatta 1020 aacagagcta ccaccaacaa cagtgtcctt cagaagcagcaactggagct gatggacaca 1080 gtccacaacc ttgtcaatct ttgcactaaa gaaggtgttttactaaaggg aggaaaaaga 1140 gaggaagaga aaccatttag agactgtgca gatgtatatcaagctggttt taataaaagt 1200 ggaatctaca ctatttatat taataatatg ccagaacccaaaaaggtgtt ttgcaatatg 1260 gatgtcaatg ggggaggttg gactgtaata caacatcgtgaagatggaag tctagatttc 1320 caaagaggct ggaaggaata taaaatgggt tttggaaatccctccggtga atattggctg 1380 gggaatgagt ttatttttgc cattaccagt cagaggcagtacatgctaag aattgagtta 1440 atggactggg aagggaaccg agcctattca cagtatgacagattccacat aggaaatgaa 1500 aagcaaaact ataggttgta tttaaaaggt cacactgggacagcaggaaa acagagcagc 1560 ctgatcttac acggtgctga tttcagcact aaagatgctgataatgacaa ctgtatgtgc 1620 aaatgtgccc tcatgttaac aggaggatgg tggtttgatgcttgtggccc ctccaatcta 1680 aatggaatgt tctatactgc gggacaaaac catggaaaactgaatgggat aaagtggcac 1740 tacttcaaag ggcccagtta ctccttacgt tccacaactatgatgattcg acctttagat 1800 ttttgaaagc gcaatgtcag aagcgattat gaaagcaacaaagaaatccg gagaagctgc 1860 caggtgagaa actgtttgaa aacttcagaa gcaaacaatattgtctccct tccagcaata 1920 agtggtagtt atgtgaagtc accaaggttc ttgaccgtgaatctggagcc gtttgagttc 1980 acaagagtct ctacttgggg tgacagtgct cacgtggctcgactatagaa aactccactg 2040 actgtcgggc tttaaaaagg gaagaaactg ctgagcttgctgtgcttcaa actactactg 2100 gaccttattt tggaactatg gtagccagat gataaatatggttaatttc 2149 2 498 PRT Homo sapiens 2 Met Thr Val Phe Leu Ser Phe AlaPhe Leu Ala Ala Ile Leu Thr His 1 5 10 15 Ile Gly Cys Ser Asn Gln ArgArg Ser Pro Glu Asn Ser Gly Arg Arg 20 25 30 Tyr Asn Arg Ile Gln His GlyGln Cys Ala Tyr Thr Phe Ile Leu Pro 35 40 45 Glu His Asp Gly Asn Cys ArgGlu Ser Thr Thr Asp Gln Tyr Asn Thr 50 55 60 Asn Ala Leu Gln Arg Asp AlaPro His Val Glu Pro Asp Phe Ser Ser 65 70 75 80 Gln Lys Leu Gln His LeuGlu His Val Met Glu Asn Tyr Thr Gln Trp 85 90 95 Leu Gln Lys Leu Glu AsnTyr Ile Val Glu Asn Met Lys Ser Glu Met 100 105 110 Ala Gln Ile Gln GlnAsn Ala Val Gln Asn His Thr Ala Thr Met Leu 115 120 125 Glu Ile Gly ThrSer Leu Leu Ser Gln Thr Ala Glu Gln Thr Arg Lys 130 135 140 Leu Thr AspVal Glu Thr Gln Val Leu Asn Gln Thr Ser Arg Leu Glu 145 150 155 160 IleGln Leu Leu Glu Asn Ser Leu Ser Thr Tyr Lys Leu Glu Lys Gln 165 170 175Leu Leu Gln Gln Thr Asn Glu Ile Leu Lys Ile His Glu Lys Asn Ser 180 185190 Leu Leu Glu His Lys Ile Leu Glu Met Glu Gly Lys His Lys Glu Glu 195200 205 Leu Asp Thr Leu Lys Glu Glu Lys Glu Asn Leu Gln Gly Leu Val Thr210 215 220 Arg Gln Thr Tyr Ile Ile Gln Glu Leu Glu Lys Gln Leu Asn ArgAla 225 230 235 240 Thr Thr Asn Asn Ser Val Leu Gln Lys Gln Gln Leu GluLeu Met Asp 245 250 255 Thr Val His Asn Leu Val Asn Leu Cys Thr Lys GluGly Val Leu Leu 260 265 270 Lys Gly Gly Lys Arg Glu Glu Glu Lys Pro PheArg Asp Cys Ala Asp 275 280 285 Val Tyr Gln Ala Gly Phe Asn Lys Ser GlyIle Tyr Thr Ile Tyr Ile 290 295 300 Asn Asn Met Pro Glu Pro Lys Lys ValPhe Cys Asn Met Asp Val Asn 305 310 315 320 Gly Gly Gly Trp Thr Val IleGln His Arg Glu Asp Gly Ser Leu Asp 325 330 335 Phe Gln Arg Gly Trp LysGlu Tyr Lys Met Gly Phe Gly Asn Pro Ser 340 345 350 Gly Glu Tyr Trp LeuGly Asn Glu Phe Ile Phe Ala Ile Thr Ser Gln 355 360 365 Arg Gln Tyr MetLeu Arg Ile Glu Leu Met Asp Trp Glu Gly Asn Arg 370 375 380 Ala Tyr SerGln Tyr Asp Arg Phe His Ile Gly Asn Glu Lys Gln Asn 385 390 395 400 TyrArg Leu Tyr Leu Lys Gly His Thr Gly Thr Ala Gly Lys Gln Ser 405 410 415Ser Leu Ile Leu His Gly Ala Asp Phe Ser Thr Lys Asp Ala Asp Asn 420 425430 Asp Asn Cys Met Cys Lys Cys Ala Leu Met Leu Thr Gly Gly Trp Trp 435440 445 Phe Asp Ala Cys Gly Pro Ser Asn Leu Asn Gly Met Phe Tyr Thr Ala450 455 460 Gly Gln Asn His Gly Lys Leu Asn Gly Ile Lys Trp His Tyr PheLys 465 470 475 480 Gly Pro Ser Tyr Ser Leu Arg Ser Thr Thr Met Met IleArg Pro Leu 485 490 495 Asp Phe 3 2269 DNA Homo sapiens 3 tgggttggtgtttatctcct cccagccttg agggagggaa caacactgta ggatctgggg 60 agagaggaacaaaggaccgt gaaagctgct ctgtaaaagc tgacacagcc ctcccaagtg 120 agcaggactgttcttcccac tgcaatctga cagtttactg catgcctgga gagaacacag 180 cagtaaaaaccaggtttgct actggaaaaa gaggaaagag aagactttca ttgacggacc 240 cagccatggcagcgtagcag ccctgcgttt cagacggcag cagctcggga ctctggacgt 300 gtgtttgccctcaagtttgc taagctgctg gtttattact gaagaaagaa tgtggcagat 360 tgttttctttactctgagct gtgatcttgt cttggccgca gcctataaca actttcggaa 420 gagcatggacagcataggaa agaagcaata tcaggtccag catgggtcct gcagctacac 480 tttcctcctgccagagatgg acaactgccg ctcttcctcc agcccctacg tgtccaatgc 540 tgtgcagagggacgcgccgc tcgaatacga tgactcggtg cagaggctgc aagtgctgga 600 gaacatcatggaaaacaaca ctcagtggct aatgaagctt gagaattata tccaggacaa 660 catgaagaaagaaatggtag agatacagca gaatgcagta cagaaccaga cggctgtgat 720 gatagaaatagggacaaacc tgttgaacca aacagctgag caaacgcgga agttaactga 780 tgtggaagcccaagtattaa atcagaccac gagacttgaa cttcagctct tggaacactc 840 cctctcgacaaacaaattgg aaaaacagat tttggaccag accagtgaaa taaacaaatt 900 gcaagataagaacagtttcc tagaaaagaa ggtgctagct atggaagaca agcacatcat 960 ccaactacagtcaataaaag aagagaaaga tcagctacag gtgttagtat ccaagcaaaa 1020 ttccatcattgaagaactag aaaaaaaaat agtgactgcc acggtgaata attcagttct 1080 tcaaaagcagcaacatgatc tcatggagac agttaataac ttactgacta tgatgtccac 1140 atcaaactcagctaaggacc ccactgttgc taaagaagaa caaatcagct tcagagactg 1200 tgctgaagtattcaaatcag gacacaccac aaatggcatc tacacgttaa cattccctaa 1260 ttctacagaagagatcaagg cctactgtga catggaagct ggaggaggcg ggtggacaat 1320 tattcagcgacgtgaggatg gcagcgttga ttttcagagg acttggaaag aatataaagt 1380 gggatttggtaacccttcag gagaatattg gctgggaaat gagtttgttt cgcaactgac 1440 taatcagcaacgctatgtgc ttaaaataca ccttaaagac tgggaaggga atgaggctta 1500 ctcattgtatgaacatttct atctctcaag tgaagaactc aattatagga ttcaccttaa 1560 aggacttacagggacagccg gcaaaataag cagcatcagc caaccaggaa atgattttag 1620 cacaaaggatggagacaacg acaaatgtat ttgcaaatgt tcacaaatgc taacaggagg 1680 ctggtggtttgatgcatgtg gtccttccaa cttgaacgga atgtactatc cacagaggca 1740 gaacacaaataagttcaacg gcattaaatg gtactactgg aaaggctcag gctattcgct 1800 caaggccacaaccatgatga tccgaccagc agatttctaa acatcccagt ccacctgagg 1860 aactgtctcgaactattttc aaagacttaa gcccagtgca ctgaaagtca cggctgcgca 1920 ctgtgtcctcttccaccaca gagggcgtgt gctcggtgct gacgggaccc acatgctcca 1980 gattagagcctgtaaacttt atcacttaaa cttgcatcac ttaacggacc aaagcaagac 2040 cctaaacatccataattgtg attagacaga acacctatgc aaagatgaac ccgaggctga 2100 gaatcagactgacagtttac agacgctgct gtcacaacca agaatgttat gtgcaagttt 2160 atcagtaaataactggaaaa cagaacactt atgttataca atacagatca tcttggaact 2220 gcattcttctgagcactgtt tatacactgt gtaaataccc atatgtcct 2269 4 496 PRT Homo sapiens 4Met Trp Gln Ile Val Phe Phe Thr Leu Ser Cys Asp Leu Val Leu Ala 1 5 1015 Ala Ala Tyr Asn Asn Phe Arg Lys Ser Met Asp Ser Ile Gly Lys Lys 20 2530 Gln Tyr Gln Val Gln His Gly Ser Cys Ser Tyr Thr Phe Leu Leu Pro 35 4045 Glu Met Asp Asn Cys Arg Ser Ser Ser Ser Pro Tyr Val Ser Asn Ala 50 5560 Val Gln Arg Asp Ala Pro Leu Glu Tyr Asp Asp Ser Val Gln Arg Leu 65 7075 80 Gln Val Leu Glu Asn Ile Met Glu Asn Asn Thr Gln Trp Leu Met Lys 8590 95 Leu Glu Asn Tyr Ile Gln Asp Asn Met Lys Lys Glu Met Val Glu Ile100 105 110 Gln Gln Asn Ala Val Gln Asn Gln Thr Ala Val Met Ile Glu IleGly 115 120 125 Thr Asn Leu Leu Asn Gln Thr Ala Glu Gln Thr Arg Lys LeuThr Asp 130 135 140 Val Glu Ala Gln Val Leu Asn Gln Thr Thr Arg Leu GluLeu Gln Leu 145 150 155 160 Leu Glu His Ser Leu Ser Thr Asn Lys Leu GluLys Gln Ile Leu Asp 165 170 175 Gln Thr Ser Glu Ile Asn Lys Leu Gln AspLys Asn Ser Phe Leu Glu 180 185 190 Lys Lys Val Leu Ala Met Glu Asp LysHis Ile Ile Gln Leu Gln Ser 195 200 205 Ile Lys Glu Glu Lys Asp Gln LeuGln Val Leu Val Ser Lys Gln Asn 210 215 220 Ser Ile Ile Glu Glu Leu GluLys Lys Ile Val Thr Ala Thr Val Asn 225 230 235 240 Asn Ser Val Leu GlnLys Gln Gln His Asp Leu Met Glu Thr Val Asn 245 250 255 Asn Leu Leu ThrMet Met Ser Thr Ser Asn Ser Ala Lys Asp Pro Thr 260 265 270 Val Ala LysGlu Glu Gln Ile Ser Phe Arg Asp Cys Ala Glu Val Phe 275 280 285 Lys SerGly His Thr Thr Asn Gly Ile Tyr Thr Leu Thr Phe Pro Asn 290 295 300 SerThr Glu Glu Ile Lys Ala Tyr Cys Asp Met Glu Ala Gly Gly Gly 305 310 315320 Gly Trp Thr Ile Ile Gln Arg Arg Glu Asp Gly Ser Val Asp Phe Gln 325330 335 Arg Thr Trp Lys Glu Tyr Lys Val Gly Phe Gly Asn Pro Ser Gly Glu340 345 350 Tyr Trp Leu Gly Asn Glu Phe Val Ser Gln Leu Thr Asn Gln GlnArg 355 360 365 Tyr Val Leu Lys Ile His Leu Lys Asp Trp Glu Gly Asn GluAla Tyr 370 375 380 Ser Leu Tyr Glu His Phe Tyr Leu Ser Ser Glu Glu LeuAsn Tyr Arg 385 390 395 400 Ile His Leu Lys Gly Leu Thr Gly Thr Ala GlyLys Ile Ser Ser Ile 405 410 415 Ser Gln Pro Gly Asn Asp Phe Ser Thr LysAsp Gly Asp Asn Asp Lys 420 425 430 Cys Ile Cys Lys Cys Ser Gln Met LeuThr Gly Gly Trp Trp Phe Asp 435 440 445 Ala Cys Gly Pro Ser Asn Leu AsnGly Met Tyr Tyr Pro Gln Arg Gln 450 455 460 Asn Thr Asn Lys Phe Asn GlyIle Lys Trp Tyr Tyr Trp Lys Gly Ser 465 470 475 480 Gly Tyr Ser Leu LysAla Thr Thr Met Met Ile Arg Pro Ala Asp Phe 485 490 495 5 495 PRT Homosapiens 5 Met Trp Gln Ile Val Phe Phe Thr Leu Ser Cys Asp Leu Val LeuAla 1 5 10 15 Ala Ala Tyr Asn Asn Phe Arg Lys Ser Met Asp Ser Ile GlyLys Lys 20 25 30 Gln Tyr Gln Val Gln His Gly Ser Cys Ser Tyr Thr Phe LeuLeu Pro 35 40 45 Glu Met Asp Asn Cys Arg Ser Ser Ser Ser Pro Tyr Val SerAsn Ala 50 55 60 Val Gln Arg Asp Ala Pro Leu Glu Tyr Asp Phe Ser Ser GlnLys Leu 65 70 75 80 Gln His Leu Glu His Val Met Glu Asn Tyr Thr Gln TrpLeu Gln Lys 85 90 95 Leu Glu Asn Tyr Ile Val Glu Asn Met Lys Ser Glu MetAla Gln Ile 100 105 110 Gln Gln Asn Ala Val Gln Asn His Thr Ala Thr MetLeu Glu Ile Gly 115 120 125 Thr Ser Leu Leu Ser Gln Thr Ala Glu Gln ThrArg Lys Leu Thr Asp 130 135 140 Val Glu Thr Gln Val Leu Asn Gln Thr SerArg Leu Glu Ile Gln Leu 145 150 155 160 Leu Glu Asn Ser Leu Ser Thr TyrLys Leu Glu Lys Gln Leu Leu Gln 165 170 175 Gln Thr Asn Glu Ile Leu LysIle His Glu Lys Asn Ser Leu Leu Glu 180 185 190 His Lys Ile Leu Glu MetGlu Gly Lys His Lys Glu Glu Leu Asp Thr 195 200 205 Leu Lys Glu Glu LysGlu Asn Leu Gln Gly Leu Val Thr Arg Gln Thr 210 215 220 Tyr Ile Ile GlnGlu Leu Glu Lys Gln Leu Asn Arg Ala Thr Thr Asn 225 230 235 240 Asn SerVal Leu Gln Lys Gln Gln Leu Glu Leu Met Asp Thr Val His 245 250 255 AsnLeu Val Asn Leu Ser Thr Lys Glu Gly Val Leu Leu Lys Gly Gly 260 265 270Lys Arg Glu Glu Glu Lys Pro Phe Arg Asp Cys Ala Asp Val Tyr Gln 275 280285 Ala Gly Phe Asn Lys Ser Gly Ile Tyr Thr Ile Tyr Ile Asn Asn Met 290295 300 Pro Glu Pro Lys Lys Val Phe Cys Asn Met Asp Val Asn Gly Gly Gly305 310 315 320 Trp Thr Val Ile Gln His Arg Glu Asp Gly Ser Leu Asp PheGln Arg 325 330 335 Gly Trp Lys Glu Tyr Lys Met Gly Phe Gly Asn Pro SerGly Glu Tyr 340 345 350 Trp Leu Gly Asn Glu Phe Ile Phe Ala Ile Thr SerGln Arg Gln Tyr 355 360 365 Met Leu Arg Ile Glu Leu Met Asp Trp Glu GlyAsn Arg Ala Tyr Ser 370 375 380 Gln Tyr Asp Arg Phe His Ile Gly Asn GluLys Gln Asn Tyr Arg Leu 385 390 395 400 Tyr Leu Lys Gly His Thr Gly ThrAla Gly Lys Gln Ser Ser Leu Ile 405 410 415 Leu His Gly Ala Asp Phe SerThr Lys Asp Ala Asp Asn Asp Asn Cys 420 425 430 Met Cys Lys Cys Ala LeuMet Leu Thr Gly Gly Trp Trp Phe Asp Ala 435 440 445 Cys Gly Pro Ser AsnLeu Asn Gly Met Phe Tyr Thr Ala Gly Gln Asn 450 455 460 His Gly Lys LeuAsn Gly Ile Lys Trp His Tyr Phe Lys Gly Pro Ser 465 470 475 480 Tyr SerLeu Arg Ser Thr Thr Met Met Ile Arg Pro Leu Asp Phe 485 490 495 6 381DNA Artificial Sequence Description of Artificial Sequence SYNTHETICOLIGONUCLEOTIDE 6 aagcttcagg tgcaactgca ggagtctgga cctgagctgg taaagcctggggcttcagtg 60 aagatgtcct gcaaggcttc tggatacaca ttcactagct atgttttccactgggtgaag 120 cagaaacctg ggcagggcct tgagtggatt ggatatatta atccttacaatgatgttact 180 aagtacaatg agaagttcaa aggcaaggcc acactgactt cagacaaatcctccagcaca 240 gcctacatgg agctcagcag cctgacctct gaggactctg cggtctattactgtgcaagc 300 tactacggta gtagttacgg atactatgct atggacgact ggggccaagggaccacggtc 360 accgtttcct ctggcggtgg c 381 7 127 PRT Artificial SequenceDescription of Artificial Sequence SYNTHETIC PEPTIDE 7 Lys Leu Gln ValGln Leu Gln Glu Ser Gly Pro Glu Leu Val Lys Pro 1 5 10 15 Gly Ala SerVal Lys Met Ser Cys Lys Ala Ser Gly Tyr Thr Phe Thr 20 25 30 Ser Tyr ValPhe His Trp Val Lys Gln Lys Pro Gly Gln Gly Leu Glu 35 40 45 Trp Ile GlyTyr Ile Asn Pro Tyr Asn Asp Val Thr Lys Tyr Asn Glu 50 55 60 Lys Phe LysGly Lys Ala Thr Leu Thr Ser Asp Lys Ser Ser Ser Thr 65 70 75 80 Ala TyrMet Glu Leu Ser Ser Leu Thr Ser Glu Asp Ser Ala Val Tyr 85 90 95 Tyr CysAla Ser Tyr Tyr Gly Ser Ser Tyr Gly Tyr Tyr Ala Met Asp 100 105 110 AspTrp Gly Gln Gly Thr Thr Val Thr Val Ser Ser Gly Gly Gly 115 120 125 8347 DNA Artificial Sequence Description of Artificial Sequence SYNTHETICOLIGONUCLEOTIDE 8 gacatccagc tgacgcagtc tccagcatcc ctgagtgtgt cagcaggagagaaggtcact 60 atgagctgca agtccagtca gagtctgtta aacagtggaa atcaaaagaactacttggcc 120 tggtatcagc agaaaccagg gcagcctcct aaactgttga tccacggggcatccactagg 180 gaatctgggg tccctgatcg cttcacaggc agtggatctg gaaccgatttcactcttacc 240 atcagcagtg tgcaggctga agacctggca gtttattact gtcagaatgattatagttat 300 cctctcacgt tcggtgctgg caccaagctg gaactgaaac gtctaga 347 9115 PRT Artificial Sequence Description of Artificial Sequence SYNTHETICPEPTIDE 9 Asp Ile Gln Leu Thr Gln Ser Pro Ala Ser Leu Ser Val Ser AlaGly 1 5 10 15 Glu Lys Val Thr Met Ser Cys Lys Ser Ser Gln Ser Leu LeuAsn Ser 20 25 30 Gly Asn Gln Lys Asn Tyr Leu Ala Trp Tyr Gln Gln Lys ProGly Gln 35 40 45 Pro Pro Lys Leu Leu Ile His Gly Ala Ser Thr Arg Glu SerGly Val 50 55 60 Pro Asp Arg Phe Thr Gly Ser Gly Ser Gly Thr Asp Phe ThrLeu Thr 65 70 75 80 Ile Ser Ser Val Gln Ala Glu Asp Leu Ala Val Tyr TyrCys Gln Asn 85 90 95 Asp Tyr Ser Tyr Pro Leu Thr Phe Gly Ala Gly Thr LysLeu Glu Leu 100 105 110 Lys Arg Leu 115 10 26 PRT Artificial SequenceDescription of Artificial Sequence SYNTHETIC PEPTIDE 10 Ala Pro Met AlaGlu Gly Gly Gly Gln Asn His His Glu Val Val Lys 1 5 10 15 Phe Met AspVal Tyr Gln Arg Ser Tyr Cys 20 25 11 25 PRT Artificial SequenceDescription of Artificial Sequence SYNTHETIC PEPTIDE 11 Ala Pro Met AlaGlu Gly Glu Gln Lys Pro Arg Glu Val Val Lys Phe 1 5 10 15 Met Asp ValTyr Lys Arg Ser Tyr Cys 20 25 12 573 DNA Artificial Sequence Descriptionof Artificial Sequence SYNTHETIC OLIGONUCLEOTIDE 12 atg cat cac cat caccat cac cat act cat cag gac ttt cag cca gtg 48 Met His His His His HisHis His Thr His Gln Asp Phe Gln Pro Val 1 5 10 15 ctc cac ctg gtg gcactg aac acc ccc ctg tct gga ggc atg cgt ggt 96 Leu His Leu Val Ala LeuAsn Thr Pro Leu Ser Gly Gly Met Arg Gly 20 25 30 atc cgt gga gca gat ttccag tgc ttc cag caa gcc cga gcc gtg ggg 144 Ile Arg Gly Ala Asp Phe GlnCys Phe Gln Gln Ala Arg Ala Val Gly 35 40 45 ctg tcg ggc acc ttc cgg gctttc ctg tcc tct agg ctg cag gat ctc 192 Leu Ser Gly Thr Phe Arg Ala PheLeu Ser Ser Arg Leu Gln Asp Leu 50 55 60 tat agc atc gtg cgc cgt gct gaccgg ggg tct gtg ccc atc gtc aac 240 Tyr Ser Ile Val Arg Arg Ala Asp ArgGly Ser Val Pro Ile Val Asn 65 70 75 80 ctg aag gac gag gtg cta tct cccagc tgg gac tcc ctg ttt tct ggc 288 Leu Lys Asp Glu Val Leu Ser Pro SerTrp Asp Ser Leu Phe Ser Gly 85 90 95 tcc cag ggt caa ctg caa ccc ggg gcccgc atc ttt tct ttt gac ggc 336 Ser Gln Gly Gln Leu Gln Pro Gly Ala ArgIle Phe Ser Phe Asp Gly 100 105 110 aga gat gtc ctg aga cac cca gcc tggccg cag aag agc gta tgg cac 384 Arg Asp Val Leu Arg His Pro Ala Trp ProGln Lys Ser Val Trp His 115 120 125 ggc tcg gac ccc agt ggg cgg agg ctgatg gag agt tac tgt gag aca 432 Gly Ser Asp Pro Ser Gly Arg Arg Leu MetGlu Ser Tyr Cys Glu Thr 130 135 140 tgg cga act gaa act act ggg gct acaggt cag gcc tcc tcc ctg ctg 480 Trp Arg Thr Glu Thr Thr Gly Ala Thr GlyGln Ala Ser Ser Leu Leu 145 150 155 160 tca ggc agg ctc ctg gaa cag aaagct gcg agc tgc cac aac agc tac 528 Ser Gly Arg Leu Leu Glu Gln Lys AlaAla Ser Cys His Asn Ser Tyr 165 170 175 atc gtc ctg tgc att gag aat agcttc atg acc tct ttc tcc aaa 573 Ile Val Leu Cys Ile Glu Asn Ser Phe MetThr Ser Phe Ser Lys 180 185 190 13 191 PRT Artificial SequenceDescription of Artificial Sequence SYNTHETIC 13 Met His His His His HisHis His Thr His Gln Asp Phe Gln Pro Val 1 5 10 15 Leu His Leu Val AlaLeu Asn Thr Pro Leu Ser Gly Gly Met Arg Gly 20 25 30 Ile Arg Gly Ala AspPhe Gln Cys Phe Gln Gln Ala Arg Ala Val Gly 35 40 45 Leu Ser Gly Thr PheArg Ala Phe Leu Ser Ser Arg Leu Gln Asp Leu 50 55 60 Tyr Ser Ile Val ArgArg Ala Asp Arg Gly Ser Val Pro Ile Val Asn 65 70 75 80 Leu Lys Asp GluVal Leu Ser Pro Ser Trp Asp Ser Leu Phe Ser Gly 85 90 95 Ser Gln Gly GlnLeu Gln Pro Gly Ala Arg Ile Phe Ser Phe Asp Gly 100 105 110 Arg Asp ValLeu Arg His Pro Ala Trp Pro Gln Lys Ser Val Trp His 115 120 125 Gly SerAsp Pro Ser Gly Arg Arg Leu Met Glu Ser Tyr Cys Glu Thr 130 135 140 TrpArg Thr Glu Thr Thr Gly Ala Thr Gly Gln Ala Ser Ser Leu Leu 145 150 155160 Ser Gly Arg Leu Leu Glu Gln Lys Ala Ala Ser Cys His Asn Ser Tyr 165170 175 Ile Val Leu Cys Ile Glu Asn Ser Phe Met Thr Ser Phe Ser Lys 180185 190 14 182 PRT Artificial Sequence Description of ArtificialSequence SYNTHETIC PEPTIDE 14 His Ser His Arg Asp Phe Gln Pro Val LeuHis Leu Val Ala Leu Asn 1 5 10 15 Ser Pro Leu Ser Gly Gly Met Arg GlyIle Arg Gly Ala Asp Phe Gln 20 25 30 Cys Phe Gln Gln Ala Arg Ala Val GlyLeu Ala Gly Thr Phe Arg Ala 35 40 45 Phe Leu Ser Ser Arg Leu Gln Asp LeuTyr Ser Ile Val Arg Arg Ala 50 55 60 Asp Arg Ala Ala Val Pro Ile Val AsnLeu Lys Asp Glu Leu Leu Phe 65 70 75 80 Pro Ser Trp Glu Ala Leu Phe SerGly Ser Glu Gly Pro Leu Lys Pro 85 90 95 Gly Ala Arg Ile Phe Ser Phe AspGly Lys Asp Val Leu Arg His Pro 100 105 110 Thr Trp Pro Gln Lys Ser ValTrp His Gly Ser Asp Pro Asn Gly Arg 115 120 125 Arg Leu Thr Glu Ser TyrCys Glu Thr Trp Arg Thr Glu Ala Pro Ser 130 135 140 Ala Thr Gly Gln AlaSer Ser Leu Leu Gly Gly Arg Leu Leu Gly Gln 145 150 155 160 Ser Ala AlaSer Cys His His Ala Tyr Ile Val Leu Cys Ile Glu Asn 165 170 175 Ser PheMet Thr Ala Ser 180 15 8 PRT Artificial Sequence Description ofArtificial Sequence SYNTHETIC PEPTIDE 15 Pro Arg Phe Lys Ile Ile Gly Gly1 5 16 8 PRT Artificial Sequence Description of Artificial SequenceSYNTHETIC PEPTIDE 16 Pro Arg Phe Arg Ile Ile Gly Gly 1 5 17 9 PRTArtificial Sequence Description of Artificial Sequence SYNTHETIC PEPTIDE17 Ser Ser Arg His Arg Arg Ala Leu Asp 1 5 18 14 PRT Artificial SequenceDescription of Artificial Sequence SYNTHETIC PEPTIDE 18 Arg Lys Ser SerIle Ile Ile Arg Met Arg Asp Val Val Leu 1 5 10 19 15 PRT ArtificialSequence Description of Artificial Sequence SYNTHETIC PEPTIDE 19 Ser SerSer Phe Asp Lys Gly Lys Tyr Lys Lys Gly Asp Asp Ala 1 5 10 15 20 15 PRTArtificial Sequence Description of Artificial Sequence SYNTHETIC PEPTIDE20 Ser Ser Ser Phe Asp Lys Gly Lys Tyr Lys Arg Gly Asp Asp Ala 1 5 10 1521 4 PRT Artificial Sequence Description of Artificial SequenceSYNTHETIC PEPTIDE 21 Ile Glu Gly Arg 1 22 4 PRT Artificial SequenceDescription of Artificial Sequence SYNTHETIC PEPTIDE 22 Ile Asp Gly Arg1 23 7 PRT Artificial Sequence Description of Artificial SequenceSYNTHETIC PEPTIDE 23 Gly Gly Ser Ile Asp Gly Arg 1 5 24 6 PRT ArtificialSequence Description of Artificial Sequence SYNTHETIC PEPTIDE 24 Pro LeuGly Leu Trp Ala 1 5 25 8 PRT Artificial Sequence Description ofArtificial Sequence SYNTHETIC PEPTIDE 25 Gly Pro Gln Gly Ile Ala Gly Gln1 5 26 8 PRT Artificial Sequence Description of Artificial SequenceSYNTHETIC PEPTIDE 26 Gly Pro Gln Gly Leu Leu Gly Ala 1 5 27 5 PRTArtificial Sequence Description of Artificial Sequence SYNTHETIC PEPTIDE27 Gly Ile Ala Gly Gln 1 5 28 8 PRT Artificial Sequence Description ofArtificial Sequence SYNTHETIC PEPTIDE 28 Gly Pro Leu Gly Ile Ala Gly Ile1 5 29 8 PRT Artificial Sequence Description of Artificial SequenceSYNTHETIC PEPTIDE 29 Gly Pro Glu Gly Leu Arg Val Gly 1 5 30 8 PRTArtificial Sequence Description of Artificial Sequence SYNTHETIC PEPTIDE30 Tyr Gly Ala Gly Leu Gly Val Val 1 5 31 8 PRT Artificial SequenceDescription of Artificial Sequence SYNTHETIC PEPTIDE 31 Ala Gly Leu GlyVal Val Glu Arg 1 5 32 8 PRT Artificial Sequence Description ofArtificial Sequence SYNTHETIC PEPTIDE 32 Ala Gly Leu Gly Ile Ser Ser Thr1 5 33 8 PRT Artificial Sequence Description of Artificial SequenceSYNTHETIC PEPTIDE 33 Glu Pro Gln Ala Leu Ala Met Ser 1 5 34 8 PRTArtificial Sequence Description of Artificial Sequence SYNTHETIC PEPTIDE34 Gln Ala Leu Ala Met Ser Ala Ile 1 5 35 8 PRT Artificial SequenceDescription of Artificial Sequence SYNTHETIC PEPTIDE 35 Ala Ala Tyr HisLeu Val Ser Gln 1 5 36 8 PRT Artificial Sequence Description ofArtificial Sequence SYNTHETIC PEPTIDE 36 Met Asp Ala Phe Leu Glu Ser Ser1 5 37 8 PRT Artificial Sequence Description of Artificial SequenceSYNTHETIC PEPTIDE 37 Glu Ser Leu Pro Val Val Ala Val 1 5 38 8 PRTArtificial Sequence Description of Artificial Sequence SYNTHETIC PEPTIDE38 Ser Ala Pro Ala Val Glu Ser Glu 1 5 39 8 PRT Artificial SequenceDescription of Artificial Sequence SYNTHETIC PEPTIDE 39 Asp Val Ala GlnPhe Val Leu Thr 1 5 40 8 PRT Artificial Sequence Description ofArtificial Sequence SYNTHETIC PEPTIDE 40 Val Ala Gln Phe Val Leu Thr Glu1 5 41 8 PRT Artificial Sequence Description of Artificial SequenceSYNTHETIC PEPTIDE 41 Ala Gln Phe Val Leu Thr Glu Gly 1 5 42 8 PRTArtificial Sequence Description of Artificial Sequence SYNTHETIC PEPTIDE42 Pro Val Gln Pro Ile Gly Pro Gln 1 5 43 31 DNA Artificial SequenceDescription of Artificial Sequence SYNTHETIC OLIGONUCLEOTIDE 43agaccatggg tcatactcat caggactttc a 31 44 29 DNA Artificial SequenceDescription of Artificial Sequence SYNTHETIC OLIGONUCLEOTIDE 44ctaccatggc tatttggaga aagaggtca 29

What is claimed is:
 1. A method of inhibiting VEGF binding to the VEGF receptor VEGFR2, without significantly inhibiting VEGF binding to the VEGF receptor VEGFR1, the method comprising contacting a cell population including cells that express VEGFR2 (KDR/Flk-1) and cells that express VEGFR1 (Flt-1) with a composition comprising a biologically effective amount of at least a first anti-VEGF antibody that binds to substantially the same epitope as the monoclonal antibody 2C3 produced by hybridoma ATCC PTA 1595, or an antigen-binding fragment of said antibody.
 2. A method of inhibiting VEGF-induced endothelial cell proliferation, comprising contacting a biological tissue comprising a population of endothelial cells with a composition comprising a biologically effective amount of at least a first anti-VEGF antibody that binds to substantially the same epitope as the monoclonal antibody 2C3 produced by hybridoma ATCC PTA 1595, or an antigen-binding fragment of said antibody.
 3. A method of inhibiting VEGF-induced endothelial cell proliferation, without significantly inhibiting VEGF stimulation of macrophages, osteoclasts or chondroclasts, comprising contacting a tissue that contains endothelial cells and at least one of macrophages, osteoclasts or chondroclasts with a composition comprising a biologically effective amount of an anti-VEGF antibody that binds to substantially the same epitope as the monoclonal antibody 2C3 produced by hybridoma ATCC PTA 1595, or an antigen-binding fragment of said antibody.
 4. A method of inhibiting angiogenesis, comprising contacting a population of potentially angiogenic blood vessels with at least a first anti-angiogenic composition comprising a biologically effective amount of at least a first anti-VEGF antibody, or antigen-binding fragment thereof, that binds to substantially the same epitope as the monoclonal antibody 2C3 produced by hybridoma ATCC PTA
 1595. 5. The method of claim 4, wherein said at least a first antibody is a monoclonal antibody or an antigen-binding fragment thereof.
 6. The method of claim 4, wherein said at least a first antibody is an IgG antibody or an IgM antibody.
 7. The method of claim 4, wherein said at least a first antibody is an scFv, Fv, Fab′, Fab, diabody, linear antibody or F(ab′)₂ antigen-binding fragment of an antibody.
 8. The method of claim 4, wherein said at least a first antibody is a dimer, trimer or multimer of said antibody or antigen-binding fragment thereof.
 9. The method of claim 4, wherein said at least a first antibody is a human, humanized or part-human antibody or antigen-binding fragment thereof.
 10. The method of claim 4, wherein said at least a first antibody is a chimeric antibody.
 11. The method of claim 4, wherein said at least a first antibody is a recombinant antibody.
 12. The method of claim 4, wherein said at least a first antibody comprises at least a first variable region that includes an amino acid sequence region having the amino acid sequence of SEQ ID NO:7 or SEQ ID NO:9.
 13. The method of claim 4, wherein said at least a first antibody is the monoclonal antibody 2C3produced by hybridoma ATCC PTA
 1595. 14. The method of claim 4, wherein said population of potentially angiogenic blood vessels is located within an animal and said at least a first anti-angiogenic composition is administered to said animal.
 15. The method of claim 14, wherein said at least a first anti-angiogenic composition is administered to said animal intravenously.
 16. The method of claim 14, wherein said animal has, or is at risk for developing, macular degeneration, age-related macular degeneration, arthritis, rheumatoid arthritis, atherosclerosis, diabetic retinopathy, thyroid hyperplasia, Grave's disease, hemangioma, neovascular glaucoma or psoriasis.
 17. The method of claim 14, wherein said animal has, or is at risk for developing, arteriovenous malformations (AVM), meningioma, vascular restenosis, angiofibroma, dermatitis, endometriosis, hemophilic joints, hypentrophic scars, inflammatory disease, pyogenic granuloma, scleroderma, synovitis, trachoma or vascular adhesions.
 18. The method of claim 14, wherein said animal has, or is at risk for developing, abnormal proliferation of fibrovascular tissue, acne rosacea, acquired immune deficiency syndrome, artery occlusion, atopic keratitis, bacterial ulcers, Bechets disease, blood borne tumors, carotid obstructive disease, chemical bums, choroidal neovascularization, chronic inflammation, chronic retinal detachment, chronic uveitis, chronic vitritis, contact lens overwear, corneal graft rejection, corneal neovascularization, corneal graft neovascularization, Crohn's disease, Eales disease, epidemic keratoconjunctivitis, fungal ulcers, Herpes simplex infections, Herpes zoster infections, hyperviscosity syndromes, Kaposi's sarcoma, leukemia, lipid degeneration, Lyme's disease, marginal keratolysis, Mooren ulcer, Mycobacteria infections other than leprosy, myopia, ocular neovascular disease, optic pits, Osler-Weber syndrome (Osler-Weber-Rendu), osteoarthritis, Pagets disease, pars planitis, pemphigoid, phylectenulosis, polyarteritis, post-laser complications, protozoan infections, pseudoxanthoma elasticum, pterygium keratitis sicca, radial keratotomy, retinal neovascularization, retinopathy of prematurity, retrolental fibroplasias, sarcoid, scleritis, sickle cell anemia, Sogrens syndrome, solid tumors, Stargarts disease, Steven's Johnson disease, superior limbic keratitis, syphilis, systemic lupus, Terrien's marginal degeneration, toxoplasmosis, trauma, tumors of Ewing sarcoma, tumors of neuroblastoma, tumors of osteosarcoma, tumors of retinoblastoma, tumors of rhabdomyosarcoma, ulceritive colitis, vein occlusion, Vitamin A deficiency or Wegeners sarcoidosis.
 19. The method of claim 14, wherein said animal has, or is at risk for developing, diabetes; parasitic disease; abnormal wound healing; hypertrophy following surgery, bums, injury or trauma; inhibition of hair growth; inhibition of ovulation and corpus luteum formation; inhibition of implantation or inhibition of embryo development in the uterus.
 20. The method of claim 14, wherein said animal has, or is at risk for developing, graft rejection, lung inflammation, nephrotic syndrome, preeclampsia, edema associated with brain tumors, ascites associated with malignancies, Meigs' syndrome, pericardial effusion, pericarditis or pleural effusion.
 21. The method of claim 14, wherein said animal has, or is at risk for developing, a vascularized solid tumor, a metastatic tumor or metastases from a primary tumor.
 22. The method of claim 21, further comprising subjecting said animal to radiotherapy.
 23. The method of claim 21, further comprising administering to said animal a therapeutically effective amount of at least a second anti-cancer agent.
 24. The method of claim 23, wherein said at least a second anti-cancer agent is administered to said animal substantially simultaneously with said at least a first antibody.
 25. The method of claim 23, wherein said at least a second anti-cancer agent is administered to said animal sequentially to said at least a first antibody.
 26. The method of claim 23, wherein said at least a second anti-cancer agent is a chemotherapeutic agent, radiotherapeutic agent, anti-angiogenic agent, apoptosis-inducing agent or anti-tubulin drug or a tumor-targeted chemotherapeutic agent, radiotherapeutic agent, anti-angiogenic agent, apoptosis-inducing agent or anti-tubulin drug.
 27. The method of claim 26, wherein said at least a second anti-cancer agent is endostatin or tumor-targeted endostatin.
 28. The method of claim 26, wherein said at least a second anti-cancer agent is an anti tubulin drug selected from the group consisting of colchicine, taxol, vinblastine, vincristine, vindescine and a combretastatin or a tumor-targeted anti-tubulin drug selected from the group consisting of colchicine, taxol, vinblastine, vincristine, vindescine and a combretastatin.
 29. The method of claim 23, wherein said at least a second anti-cancer agent is a targeting agent-therapeutic agent construct comprising a therapeutic agent operatively linked to at least a first targeting region that binds to an accessible component of a tumor cell, tumor stroma or tumor vasculature.
 30. The method of claim 29, wherein said at least a first targeting region binds to a surface-expressed, surface-accessible, surface-localized, cytokine-inducible or coagulant-inducible component of intratumoral blood vessels of a vascularized tumor.
 31. The method of claim 29, wherein said at least a first targeting region is operatively linked to a cytotoxic agent, anti-angiogenic agent, apoptosis-inducing agent or anti-tubulin drug.
 32. The method of claim 31, wherein said at least a first targeting region is operatively linked to deglycosylated ricin A chain or gelonin.
 33. The method of claim 29, wherein said at least a first targeting region is operatively linked to a coagulant or to an antibody, or antigen-binding fragment thereof, that binds to a coagulant.
 34. The method of claim 33, wherein said at least a first targeting region is operatively linked to Tissue Factor, truncated Tissue Factor or a Tissue Factor derivative or to an antibody, or antigen-binding fragment thereof, that binds to Tissue Factor, truncated Tissue Factor or a Tissue Factor derivative.
 35. The method of claim 14, wherein said animal is a human patient.
 36. A method for treating an animal that has, or is at risk for developing, a vascularized solid tumor, a metastatic tumor or metastases from a primary tumor, comprising administering to said animal at least a first pharmaceutical composition that comprises at least a first purified, unconjugated anti-VEGF antibody, or an antigen-binding fragment thereof, that binds to the same epitope as the monoclonal antibody 2C3 produced by hybridoma ATCC PTA 1595 and that significantly inhibits VEGF binding to the VEGF receptor VEGFR2 (KDR/Flk-1) without significantly inhibiting VEGF binding to the VEGF receptor VEGFR1 (Flt-1).
 37. A method for treating cancer, comprising administering to an animal with a vascularized tumor a therapeutically effective amount of at least a first pharmaceutical composition that comprises at least a first unconjugated anti-VEGF antibody that binds to substantially the same epitope as the monoclonal antibody 2C3 produced by hybridoma ATCC PTA 1595, or an antigen-binding fragment thereof; wherein said anti-VEGF antibody substantially inhibits VEGF binding to the VEGF receptor VEGFR2 (KDR/Flk- 1) without significantly inhibiting VEGF binding to the VEGF receptor VEGFR1 (Flt-1), thereby inhibiting angiogenesis within said vascularized tumor without significantly impairing macrophage-mediated anti-tumor responses within said vascularized tumor.
 38. A method for treating cancer, comprising administering to an animal with a vascularized tumor a therapeutically effective amount of at least a first pharmaceutical composition that comprises at least a first naked anti-VEGF antibody that binds to substantially the same epitope as the monoclonal antibody 2C3 produced by hybridoma ATCC PTA 1595, or an antigen-binding fragment thereof; wherein said anti-VEGF antibody substantially inhibits VEGF binding to the VEGF receptor VEGFR2 (KDR/Flk-1) without significantly inhibiting VEGF binding to the VEGF receptor VEGFR1 (Flt-1), thereby inhibiting angiogenesis within said vascularized tumor without significantly inhibiting VEGF stimulation of macrophages, osteoclasts or chondroclasts within said animal.
 39. The method of claim 4, wherein said at least a first anti-VEGF antibody, or antigen-binding fragment thereof, binds to the same epitope as the monoclonal antibody 2C3 produced by hybridoma ATCC PTA
 1595. 40. A method of inhibiting angiogenesis, comprising contacting a population of potentially angiogenic blood vessels with at least a first anti-angiogenic composition comprising a biologically effective amount of at least a first purified, unconjugated anti-VEGF antibody, or an antigen-binding fragment thereof, that binds to the same epitope as the monoclonal antibody 2C3 produced by hybridoma ATCC PTA
 1595. 